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Telmisartan

  • Prescription medicine
  • Prescription only
  • Identity checked
  • Sources last checked 2026-09-04

This page shows what was measured, who it was measured in, and what that does not settle.

What Telmisartan does in the body

Hypertension, to lower blood pressure

From the FDA-approved label: Angiotensin II is formed from angiotensin I in a reaction catalyzed by angiotensin-converting enzyme (ACE, kininase II). Angiotensin II is the principal pressor agent of the renin-angiotensin system, with effects that include vasoconstriction, stimulation of synthesis and release of aldosterone, cardiac stimulation, and renal reabsorption of sodium. Telmisartan blocks the vasoconstrictor and aldosterone-secreting effects of angiotensin II by selectively blocking the binding of angiotensin II to the AT 1 receptor in many tissues, such as vascular smooth muscle and the adrenal gland. Its action is therefore independent of the pathways for angiotensin II synthesis.

What happened in people

RNAWiki has not yet published a reviewed conclusion for this use.

A fixed RNAWiki sentence

Where this came from

Wording RNAWiki always uses, not a finding about this substance.

No reviewed claim names a result for any goal on this record.

No source is stored against this line.

The limit that matters most

Not recorded.

Where it acts
Not recorded.
Kind of result
No result is published, so no kind of result applies yet
Supervision
Professional supervision is normally required. A regulator classifies this substance in a way that restricts how it is supplied.

What the registries record it as

  • The substance registry classes this as chemical.

    FDA substance registry · U5SYW473RQ · read 2026-08-29

  • Its recorded molecular formula is C33H30N4O2, weighing 514.63.

    US prescribing information · a075633a-2a2a-4e88-8ede-b49a3920a16c · read 2026-08-30

Where each sentence above came from

No recorded sentence describes the change this makes in a way that stands on its own. The page opens with what it is taken for instead, and the recorded explanation follows below.

Shown as the opening line on this page.

No statement of the main limit is recorded.

The four opening statements run to 116 words.

Words this page uses

Four words worth knowing first

Chosen from what this page shows, with each one explained before the word it depends on.

Stand-in result

A stand-in result is a number measured because the real result takes too long.

A picture of it, and where the picture fails

It is like judging a journey by the speedometer rather than by arriving.

Where that stops being true. Speed does predict arrival. Many stand-in results do not predict the real one.

What people get wrong. A stand-in result is often reported as the result itself.

A surrogate endpoint substituted for a clinical endpoint, valid only where the substitution has been shown to hold.

Enzyme

An enzyme is a protein that speeds up one chemical change.

A picture of it, and where the picture fails

An enzyme is like a machine on a production line doing one cut.

Where that stops being true. A machine is switched on and off by a person. Enzymes are controlled by the cell.

What people get wrong. Enzymes are thought to be used up. They are not; they work again and again.

A catalytic protein that lowers the activation energy of a specific reaction.

Receptor

A receptor is a part of a cell that a signal fits into.

A picture of it, and where the picture fails

A receptor is like a lock waiting for one key.

Where that stops being true. A lock either opens or does not. A receptor can be half-triggered, or worn out.

What people get wrong. Fitting a receptor is read as causing a benefit. It causes a step, and nothing more.

A protein that binds a specific ligand and converts that binding into a cellular response.

Pathway

A pathway is a chain of steps inside a cell, each one setting off the next.

A picture of it, and where the picture fails

A pathway is like a row of dominoes.

Where that stops being true. Dominoes fall one way. Pathways loop back and can switch themselves off.

What people get wrong. Changing one step is read as changing the outcome. Other steps often absorb it.

An ordered series of molecular interactions producing a defined cellular change.

What happened in peopleRead from sources, not yet reviewed

What was measured, goal by goal

One row for each goal a registered study measured something for. One column for each kind of thing that could be measured.

Registered studies list 40 outcome measures that RNAWiki could read. A registered study says what someone planned to measure. It does not say what they found. 0 of the matched studies tested this substance, and 0 posted a result.

There is no single score. A strong test result and a weak life result are different facts.

Goals down the side, kinds of measurement across the top. Each cell says what kind of thing was registered, not what was found.
GoalLife outcomeWhat a body can doHow a person feelsA test resultA step in the bodyHarmsHow longWho was studied
CholesterolNothing in the sources checkedNo registered study lists a life outcome for this goal.Nothing in the sources checkedNo registered study lists a performance measure for this goal.Nothing in the sources checkedNo registered study lists a symptom measure for this goal.Only a number moved4 registered test measure.Nothing in the sources checkedNo registered study lists a body-step measure for this goal.Not recordedHarms were not a registered measure for this goal.Not recordedNo finished study window is recorded.Waiting for a reviewerWho was studied is listed further down the page.
Blood sugarNothing in the sources checkedNo registered study lists a life outcome for this goal.Nothing in the sources checkedNo registered study lists a performance measure for this goal.Nothing in the sources checkedNo registered study lists a symptom measure for this goal.Only a number moved3 registered test measure.Nothing in the sources checkedNo registered study lists a body-step measure for this goal.Not recordedHarms were not a registered measure for this goal.Not recordedNo finished study window is recorded.Waiting for a reviewerWho was studied is listed further down the page.
Healthy ageingWaiting for a reviewer1 registered study measure of this kind. No reviewed result yet.Nothing in the sources checkedNo registered study lists a performance measure for this goal.Nothing in the sources checkedNo registered study lists a symptom measure for this goal.Nothing in the sources checkedNo registered study lists a test result for this goal.Nothing in the sources checkedNo registered study lists a body-step measure for this goal.Not recordedHarms were not a registered measure for this goal.Not recordedNo finished study window is recorded.Waiting for a reviewerWho was studied is listed further down the page.
Which registered measures put each goal on this table
Cholesterol
metabolic profiles including lipid profile and blood glucose; control of blood pressure and decline in triglycerides level; triglycerides; diastolic blood pressure change in ldl cholesterol
Blood sugar
metabolic profiles including lipid profile and blood glucose; insulin resistance; insulin sensitivity
Healthy ageing
mortality

Sorted by fixed word lists, version v1. A name the rules do not recognise stays unsorted rather than moving to the nearest column.

What each mark on this table means
Nothing in the sources checked
No registered study lists a life outcome for this goal.
Only a number moved
4 registered test measure.
Not recorded
Harms were not a registered measure for this goal.
Waiting for a reviewer
Who was studied is listed further down the page.

What happened in peopleRead from sources, not yet reviewed

What happened in people

Each card is one study: the exact question it asked, who was in it, and whether it showed what it set out to show.

ONTARGET. Composite Endpoint of Cardiovascular Death, Non-fatal Myocardial Infarction, Non-fatal Stroke and Hospitalization for Congestive Heart Failure

The study did not show it

Who was studied
NCT00153101
How many people
31546
Study design
Phase 4
Compared against
Not recorded for this study
Kind of result
Living longer, or avoiding a major event
What was found
Result not recorded on this page
Repeated elsewhere
Unreplicated

What this does not prove. A study that did not show an effect does not show that no effect exists anywhere.

The limits of this study, and where it came from

Main limit. No limitation is recorded for this study.

How far it carries. This study is recorded from the curated record, not from the registry match.

Form and route. Oral

Interval reported. Not recorded in this summary

Written into the record, not signed off as a reviewed claim.

  • openFDA Drugs@FDA · a recorded source, not a stored snapshot
  • openFDA NDC Directory · a recorded source, not a stored snapshot
  • openFDA SPL label · a recorded source, not a stored snapshot
  • PubChem PUG-REST · a recorded source, not a stored snapshot

To evaluate the impact of circadian time of treatment in cardiovascular, cerebrovascular, metabolic, and renal risk assessment.

The study did not show it

Who was studied
NCT00741585
How many people
21983
Study design
Phase 4
Compared against
Not recorded for this study
Kind of result
A number that stands in for health
What was found
Result not recorded on this page
Repeated elsewhere
Unreplicated

What this does not prove. A study that did not show an effect does not show that no effect exists anywhere.

The limits of this study, and where it came from

Main limit. No limitation is recorded for this study.

How far it carries. This study is recorded from the curated record, not from the registry match.

Form and route. Oral

Interval reported. Not recorded in this summary

Written into the record, not signed off as a reviewed claim.

  • openFDA Drugs@FDA · a recorded source, not a stored snapshot
  • openFDA NDC Directory · a recorded source, not a stored snapshot
  • openFDA SPL label · a recorded source, not a stored snapshot
  • PubChem PUG-REST · a recorded source, not a stored snapshot

Number of Patients With First Recurrent Stroke of Any Type, Fatal or Nonfatal (Antiplatelet Comparison Only)

The study did not show it

Who was studied
NCT00153062
How many people
20332
Study design
Phase 4
Compared against
Not recorded for this study
Kind of result
A number that stands in for health
What was found
Result not recorded on this page
Repeated elsewhere
Unreplicated

What this does not prove. A study that did not show an effect does not show that no effect exists anywhere.

The limits of this study, and where it came from

Main limit. No limitation is recorded for this study.

How far it carries. This study is recorded from the curated record, not from the registry match.

Form and route. Oral

Interval reported. Not recorded in this summary

Written into the record, not signed off as a reviewed claim.

  • openFDA Drugs@FDA · a recorded source, not a stored snapshot
  • openFDA NDC Directory · a recorded source, not a stored snapshot
  • openFDA SPL label · a recorded source, not a stored snapshot
  • PubChem PUG-REST · a recorded source, not a stored snapshot

All-cause mortality

The study did not show it

Who was studied
NCT02735707
How many people
20000
Study design
Phase 3
Compared against
Not recorded for this study
Kind of result
Living longer, or avoiding a major event
What was found
Result not recorded on this page
Repeated elsewhere
Unreplicated

What this does not prove. A study that did not show an effect does not show that no effect exists anywhere.

The limits of this study, and where it came from

Main limit. No limitation is recorded for this study.

How far it carries. This study is recorded from the curated record, not from the registry match.

Form and route. Oral

Interval reported. Not recorded in this summary

Written into the record, not signed off as a reviewed claim.

  • openFDA Drugs@FDA · a recorded source, not a stored snapshot
  • openFDA NDC Directory · a recorded source, not a stored snapshot
  • openFDA SPL label · a recorded source, not a stored snapshot
  • PubChem PUG-REST · a recorded source, not a stored snapshot

The primary study outcomes are composite of non-fatal stroke, non-fatal myocardial infarction and cardiovascular death.

The study did not show it

Who was studied
NCT01011660
How many people
13542
Study design
Phase 4
Compared against
Not recorded for this study
Kind of result
Living longer, or avoiding a major event
What was found
Result not recorded on this page
Repeated elsewhere
Unreplicated

What this does not prove. A study that did not show an effect does not show that no effect exists anywhere.

The limits of this study, and where it came from

Main limit. No limitation is recorded for this study.

How far it carries. This study is recorded from the curated record, not from the registry match.

Form and route. Oral

Interval reported. Not recorded in this summary

Written into the record, not signed off as a reviewed claim.

  • openFDA Drugs@FDA · a recorded source, not a stored snapshot
  • openFDA NDC Directory · a recorded source, not a stored snapshot
  • openFDA SPL label · a recorded source, not a stored snapshot
  • PubChem PUG-REST · a recorded source, not a stored snapshot

the prevention of recurrent stroke.

The study did not show it

Who was studied
NCT01198496
How many people
5000
Study design
Phase 4
Compared against
Not recorded for this study
Kind of result
A number that stands in for health
What was found
Result not recorded on this page
Repeated elsewhere
Unreplicated

What this does not prove. A study that did not show an effect does not show that no effect exists anywhere.

The limits of this study, and where it came from

Main limit. No limitation is recorded for this study.

How far it carries. This study is recorded from the curated record, not from the registry match.

Form and route. Oral

Interval reported. Not recorded in this summary

Written into the record, not signed off as a reviewed claim.

  • openFDA Drugs@FDA · a recorded source, not a stored snapshot
  • openFDA NDC Directory · a recorded source, not a stored snapshot
  • openFDA SPL label · a recorded source, not a stored snapshot
  • PubChem PUG-REST · a recorded source, not a stored snapshot
What we know
RNAWiki holds 6 written-up human studies for this substance, each with the question it asked.
How we know it
Each card names the study, the number of people and what the study set out to measure.
What this does not prove
These summaries were written by a person and have not been signed off as reviewed claims.
Why it matters
A study that failed is as informative as one that worked, and both are here.
What we still do not know
No reviewed claim exists, so no exact population, effect size or interval is published yet.

What happened in peopleRead from sources, not yet reviewed

How close this is to real life

The top step is something a person would feel or care about. The bottom is a guess from software. Filled steps are where evidence exists for this substance.

  1. Living longer, or avoiding a major event Evidence recorded. Death, a heart attack, a stroke, a hospital stay.3 registered measures of this kind. 2 written-up studies measured this and did not show a benefit.
  2. What a body can do day to day No evidence recorded. Walking, dressing, breathing, recovering.No registered study measures this.
  3. Measured performance No evidence recorded. How much was lifted, how far was run, how fast.No registered study measures this.
  4. Symptoms and quality of life No evidence recorded. Pain, tiredness, mood, sleep, as the person rated it.No registered study measures this.
  5. A number that stands in for health Evidence recorded. Cholesterol, blood sugar, bone density. A stand-in, not the thing itself.22 registered measures of this kind.
  6. A step measured inside a person Evidence recorded. Something measured in human tissue or human cells.A human record sits on the stored organism ladder.
  7. Animals Evidence recorded. Mice, rats, dogs. Useful for ideas, not proof about people.Stored records in Mouse, Rat. A result in animals says what to test next. It does not say what happens in people.
  8. Cells in a dish Evidence recorded. Cells or chemistry on a bench, far from a whole body.Stored mechanism abstracts describe steps measured in cells or tissue.
  9. A guess from software No evidence recorded. Nobody measured it. RNAWiki never publishes one as a finding.RNAWiki stores no prediction for this record. Software can suggest a link. RNAWiki does not publish one as a finding.

Higher on these steps means closer to something a person would feel. It does not mean better done.

What it would be like to takeRead from sources, not yet reviewed

Felt, measured, or meaningful

Three different things that get called the same word. Registered studies measured all three, and mixing them is how a blood test becomes a health claim.

Felt

Things a person could notice without a test.

No registered study measured anything of this kind.

Measured

Things only a test, a scale or a device shows.

  • supine diastolic blood pressure at trough
  • home blood pressure in the early morning
  • blood pressure surge in the morning
  • blood pressure
  • metabolic profiles including lipid profile and blood glucose
  • high sensitivity c reactive protein
  • trough seated systolic blood pressure at week 8
  • seated trough cuff systolic blood pressure to week 7
  • control of blood pressure and decline in triglycerides level
  • insulin resistance

and 12 more.

Meaningful

Things that change how a life goes, not only a number.

  • first recurrent stroke of any type fatal or nonfatal
  • prevention of recurrent stroke
  • mortality

A registered study says what someone planned to measure. It does not say what they found. A number moving is not the same as a life going better. The two are shown apart here.

Felt, but not shown to help. A person notices a change. No study showed it leads anywhere good.

Measured, but not felt. A number moves. The person notices nothing. Both can be true.

Measured, but not shown to matter. A number moves in the good direction. Nobody showed that lives went better.

Matters, but takes years. The result that counts may take longer than anyone would keep watching.

Names that fit none of the three (15)
  • after one year of treatment in proteinuria
  • glomerular filtration rate gfr after five years of treatment
  • at 8 weeks in seated trough cuff mean dbp
  • seated trough cuff mean dbp
  • study a annual change in total kidney volume
  • incidence of adverse events
  • changes in electrocardiogram
  • homa index
  • il 6
  • efficacy
  • visceral adipose tissue volume
  • auc0 tz
  • cmax
  • recurrence of atrial fibrillation
  • part b auc cmax of chlorthalidone

These are harms, study-process measures, or names the rules did not recognise. They are shown rather than dropped.

What it would be like to takeRead from sources, not yet reviewed

How long anything takes

Nine different lengths of time that get confused with each other. None of them is worked out from another.

  1. Before anything is noticed. RNAWiki does not store this separately, and never works it out from another figure on this page.

  2. Before a test result moves. RNAWiki does not store this separately, and never works it out from another figure on this page.

  3. Before performance moves. RNAWiki does not store this separately, and never works it out from another figure on this page.

  4. How long the result was watched. No finished study window is recorded for a study that tested this substance.

  5. How long people took it. How long people actually took it is not stored. The study window is not the same thing.

  6. How long people were followed. Follow-up length is not stored separately. It is never read off the study window, which would be a different thing.

  7. How fast the body clears it. 24 hours hours

    Read from the label, which states: “Telmisartan shows bi-exponential decay kinetics with a terminal elimination half-life of approximately 24 hours.”

  8. How long effects linger. RNAWiki does not store this separately, and never works it out from another figure on this page.

  9. Beyond the studies. Nothing is recorded about the long term.

    The longest finished study sets the edge of what anyone measured.

A study window is not how long people took it, and neither is how long they were followed. Where RNAWiki holds only one of the three, it shows one.

What is missing or unclearRead from sources, not yet reviewed

Were people like you studied?

RNAWiki cannot tell whether a study fits you. It can show who was in it, and where the result stops carrying.

Who was studied

People similar to this profile were included.

  • Telmisartan is an angiotensin II receptor blocker (ARB) indicated for: • Treatment of hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions.( 1.1 ) • Cardiovascular (CV) risk reduction in patients unable to take ACE inhibitors (1.2) 1.1 Hypertension Telmisartan tablets,USP are indicated for the…

Who is missing from the studies

  • Which groups were under-represented in the studies has not been recorded for this substance. Pregnancy, breastfeeding, children, older adults, and people with liver or kidney conditions are commonly excluded from trials; nothing here says whether they were.

What the label states about particular groups

  • On pediatric, the label states: “Safety and effectiveness in pediatric patients have not been established [ see Clinical Pharmacology ( 12.3) ].”

    US prescribing information · a075633a-2a2a-4e88-8ede-b49a3920a16c · read 2026-08-30

  • On older people, the label states: “Of the total number of patients receiving telmisartan in hypertension clinical studies, 551 (19%) were 65 to 74 years of age and 130 (4%) were 75 years or older.”

    US prescribing information · a075633a-2a2a-4e88-8ede-b49a3920a16c · read 2026-08-30

  • On people who are pregnant, the label states: “Risk Summary Telmisartan can cause fetal harm when administered to a pregnant woman.”

    US prescribing information · a075633a-2a2a-4e88-8ede-b49a3920a16c · read 2026-08-30

  • On people who are breastfeeding, the label states: “Risk Summary There is no information regarding the presence of telmisartan in human milk, the effects on the breastfed infant, or the effects on milk production.”

    US prescribing information · a075633a-2a2a-4e88-8ede-b49a3920a16c · read 2026-08-30

Where the result stopped carrying

  • This is a scope explorer, not a diagnosis engine.
  • It shows who was studied so you can see whether people similar to you were included.

RNAWiki cannot tell whether a study fits you. It can show who was in it.

What it would be like to takeRead from sources, not yet reviewed

Why it might seem to do nothing

A real effect and a noticed effect are different things. These are the recorded reasons the two come apart.

It was studied for a different goal

The studies measured something else entirely.

On this record: Some registered studies measured things that match no goal on this page.

It was studied in different people

The people in the studies were not much like the reader.

On this record: Which groups were under-represented in the studies has not been recorded for this substance. Pregnancy, breastfeeding, children, older adults, and people with liver or kidney conditions are commonly excluded from trials; nothing here says whether they were.

The evidence may simply be wrong

Small early studies often do not hold up.

On this record: RNAWiki has not yet published a reviewed conclusion for this use.

Other reasons RNAWiki checked and found nothing for (10)
A different form was studied
The studied form is not the form on the shelf. Nothing in this record points to this reason.
There was nothing to correct
Where a level is already normal, topping it up may change nothing. Nothing in this record points to this reason.
Something else had to happen too
In the studies it was paired with training, a diet or another treatment. Nothing in this record points to this reason.
The change is too small to feel
A real change can still sit below what a person notices. Nothing in this record points to this reason.
Day-to-day swing hides it
Sleep, food, stress and time of day move most numbers more than this would. Nothing in this record points to this reason.
Not enough time yet
The studies ran longer than the person has waited. Nothing in this record points to this reason.
It was not taken as studied
Missed days change the result, and studies count them. Nothing in this record points to this reason.
Something else changed at the same time
Two changes at once cannot be told apart afterwards. Nothing in this record points to this reason.
The product may not be what it says
Contents of a sold product are not always what the label states. Nothing in this record points to this reason.
No recorded reason
RNAWiki has nothing stored that would explain it. Nothing in this record points to this reason.

None of these is a reason to take more. Taking more is not a step this page ever suggests.

What it would be like to takeRead from sources, not yet reviewed

What taking it involves

The recorded facts about getting hold of it and using it. Nothing here is a suggestion about what you should do.

How it is supplied

Prescription only

Quoted from a source

Where this came from

Copied from a source RNAWiki stored, with the source named.

Read from the recorded approval status.

No source is stored against this line.

Form and route

Oral

Source-linked record

Where this came from

A person wrote this into the record with the study named beside it. No reviewer has signed it off.

The form and route recorded on this substance.

No source is stored against this line.

Who oversees it

Professional supervision is normally required. A regulator classifies this substance in a way that restricts how it is supplied.

Quoted from a source

Where this came from

Copied from a source RNAWiki stored, with the source named.

Suppression classes recorded: S3, S6.

No source is stored against this line.

What is in the pack

Sold as tablet, given by the oral route.

Source-linked record

Where this came from

A person wrote this into the record with the study named beside it. No reviewer has signed it off.

Recorded notes on how this is sold and what that means for what is in the pack.

No source is stored against this line.

Where it is registered

Regulatory records are listed in the technical disclosure at the foot of this page.

Counted from records

Where this came from

A count of rows RNAWiki holds. It describes our records, not your body.

Register entries are stored per jurisdiction and shown with their dates.

No source is stored against this line.

Why people stop

Not recorded.

Nothing recorded

Where this came from

RNAWiki holds nothing here and says so rather than guessing.

No record of why people stopped taking it is stored for this substance.

No source is stored against this line.

What it would be like to takeNothing found in the sources checked

What can go wrong

Sorted by where each line came from. A regulator's label and a report somebody sent in are not the same kind of fact.

Nothing found in the sources checked

No harm is recorded against this substance in the sources RNAWiki checked. Finding nothing is not the same as showing there is nothing.

The sources listed were searched and held nothing. That is not the same as nothing existing.

Reports sent to a regulator

  • These are reports people sent to a regulator. They do not show the medicine caused the reaction.
  • Nobody counted how many people took the medicine and reported nothing.
  • The same event can be reported more than once, and many reports are incomplete.
  • News coverage, lawsuits and new warnings change how often people report.
  • A count is not a rate and not a risk.

Telmisartan appears in spontaneous reports to regulators. Across the 10 most-reported reaction terms, 1568 reaction mentions were counted. One report can name several reactions.

The recorded terms (10)
  • hypotension — 233 reaction mentions
  • hyponatraemia — 219 reaction mentions
  • acute kidney injury — 168 reaction mentions
  • hypertension — 165 reaction mentions
  • blood pressure increased — 162 reaction mentions
  • hyperkalaemia — 159 reaction mentions
  • loss of consciousness — 129 reaction mentions
  • renal failure acute — 129 reaction mentions
  • renal failure — 111 reaction mentions
  • suicide attempt — 93 reaction mentions
  • open-targets-adr · recorded 2026-06-24 · a recorded source, not a stored snapshot

Over a long time. No completed tested study window is recorded, so long-term effects are not established by the registry record.

Groups the studies covered thinly. Which groups were under-represented in the studies has not been recorded for this substance. Pregnancy, breastfeeding, children, older adults, and people with liver or kidney conditions are commonly excluded from trials; nothing here says whether they were.

What is missing or unclearRead from sources, not yet reviewed

Does the exact form matter?

Evidence belongs to the exact thing that was tested. A different salt, a different mixture or a different preparation is a different question.

The form that was studied

Oral

Source-linked record

Where this came from

A person wrote this into the record with the study named beside it. No reviewer has signed it off.

The form used in the studies cited on this page.

No source is stored against this line.

What is sold

Not recorded.

Nothing recorded

Where this came from

RNAWiki holds nothing here and says so rather than guessing.

Nothing further is recorded about which forms are sold.

No source is stored against this line.

What is recorded as being sold

  • 152 products list this as an active ingredient in the United States drug directory. 106 of them contain it and nothing else.

    FDA National Drug Code directory · 72162-2438 · read 2026-08-29

  • They are sold as granule, powder and tablet, taken oral.

    FDA National Drug Code directory · 72162-2438 · read 2026-08-29

  • The regulator's established pharmacologic class for it is angiotensin 2 receptor antagonists [moa] and angiotensin 2 receptor blocker [epc].

    FDA National Drug Code directory · 72162-2438 · read 2026-08-29

  • 55 published labels name it as an active ingredient. 42 of them describe this substance alone, which is where its own label text on this page comes from.

    US prescribing information · 2e3cc412-fa44-4304-aabc-d6e412f81fbf · read 2026-08-29

  • Those labels are classed as human prescription drug.

    US prescribing information · 2e3cc412-fa44-4304-aabc-d6e412f81fbf · read 2026-08-29

  • Telmisartan is oral at 3 DOSAGE FORMS AND STRENGTHS • 20 mg, white to off-white, round shaped, uncoated tablet, debossed with "C44" on one side and plain on other side. • 40 mg, white to off-white, oblong, biconvex, uncoated tablet, debossed…, recorded as fda label in effect 2023-09-30 in the United States.

    US prescribing information · a075633a-2a2a-4e88-8ede-b49a3920a16c · read 2026-08-30

  • Recorded price in US: 0.10387–0.15626 USD per one unit as the pricing file counts it — a tablet, capsule, patch or single item, across 62 priced products whose strengths and pack forms differ, as of 2026-08-26, paid by retail pharmacies buying the product, as surveyed by the Centers for Medicare & Medicaid Services. It is not a list price, an insurance price, or what anyone pays at a counter..

    Recorded source · 2026-08-26 · read 2026-08-28

Evidence carries across two names for one substance. It does not carry across a salt, a mirror form or a mixture.

What it would be like to takeRead from sources, not yet reviewed

What you could measure

This one is decided with a clinician, so this section holds questions to ask rather than a plan to run.

Self-experiment planning is not offered for a prescription or clinician-supervised medicine. The questions below are for a clinician or pharmacist.

Questions worth asking

  • Which of the trials of Telmisartan studied people like me?
  • What was measured, and for how long?
  • Was the result a laboratory value or a health outcome?
  • What would we watch for, and when would we stop?

Tracking can show whether something changed for you. It cannot show what caused it.

RNAWiki records evidence. It does not say whether this substance is right for you.

What is missing or unclearRead from sources, not yet reviewed

What nobody knows yet

Open questions, each with why it is open and what would close it.

Missing populations

Which groups were under-represented in the studies has not been recorded.

Why it matters. Recorded by the evidence model as a gap on this record.

What would answer it

A study that measures it, and a reviewer to sign it off.

Last checked 2026-09-04. Searched: The sources listed in the receipts at the foot of this page.

Missing long-term data

No completed tested study window is recorded.

Why it matters. Recorded by the evidence model as a gap on this record.

What would answer it

A study that measures it, and a reviewer to sign it off.

Last checked 2026-09-04. Searched: The sources listed in the receipts at the foot of this page.

No reviewed conclusion

RNAWiki has not yet published a reviewed conclusion for this use.

Why it matters. Recorded by the evidence model as a gap on this record.

What would answer it

A study that measures it, and a reviewer to sign it off.

Last checked 2026-09-04. Searched: The sources listed in the receipts at the foot of this page.

Missing interaction studies

No interaction was found in the registers checked. Not finding one is not the same as showing there is none.

Why it matters. Recorded by the evidence model as a gap on this record.

What would answer it

A study that measures it, and a reviewer to sign it off.

Last checked 2026-09-04. Searched: The sources listed in the receipts at the foot of this page.

Formulation uncertainty

Several salts, forms or products of Telmisartan are recorded. Results from one form may not transfer to another.

Why it matters. Recorded by the evidence model as a gap on this record.

What would answer it

A study that measures it, and a reviewer to sign it off.

Last checked 2026-09-04. Searched: The sources listed in the receipts at the foot of this page.

Mechanism not reviewed

No reviewed mechanism story exists for this substance.

Why it matters. Recorded by the evidence model as a gap on this record.

What would answer it

A study that measures it, and a reviewer to sign it off.

Last checked 2026-09-04. Searched: The sources listed in the receipts at the foot of this page.

What happened in peopleRead from sources, not yet reviewed

Check any of this yourself

Every line above traced back to the study it came from. This is the technical layer, and the vocabulary changes here.

How many documents were read

  • 41 documents were read for this substance.

    RNAWiki source record

  • 38 of them state the same halfLife, and they agree.

    RNAWiki source record

  • 41 of them state the same bioavailability, and they agree.

    RNAWiki source record

  • 41 of them state the same tMax, and they agree.

    RNAWiki source record

  • 41 of them state the same proteinBinding, and they agree.

    RNAWiki source record

Where else this substance is registered

FDA substance identifier (UNII)
U5SYW473RQ
RxNorm concept
205304

Checks this page had to pass

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  • Not passed

    Trial roles classified for highlighted evidence

    No registered study is classified as testing this substance.

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    Safety mode resolved

    Suppression classes recorded: S3, S6.

  • Passed

    Canonical metadata present

    slug and display name present

What is missing or unclearRead from sources, not yet reviewed

How this medicine reached us

Kept near the foot of the page. A historical event moves up only when it changes something about this substance today.

What the approval register records

  • 37 approved applications cover products containing this substance. The earliest was NDA020850, approved 19981110 to BOEHRINGER INGELHEIM.

    Drugs@FDA application register · NDA020850 · read 2026-08-29

  • Marketing status on the register: discontinued, none (tentative approval) and prescription.

    Drugs@FDA application register · NDA020850 · read 2026-08-29

  • The earliest marketing start date recorded for a listed product is 20001201.

    FDA National Drug Code directory · 72162-2438 · read 2026-08-29

What is missing or unclearRead from sources, not yet reviewed

What to learn next

Ordered by what would most change how you read this page, starting with what is easiest to misunderstand.

This order is fixed in code and does not count clicks or time on the page.

What is not here

5 questions this page could not answer

These sections were prepared and left out because there was nothing to put in them. They are listed rather than hidden, so the gaps in this record are visible.

  • The path through the body — found nothing in the sources checked.
  • What it may clash with — found nothing in the sources checked.
  • Other ways to the same goal — found nothing in the sources checked.
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The record as stored

The full record, for auditing

Everything above is built from what is below. This layer keeps the technical vocabulary, record identifiers and every stored row, so a reader who wants to check the page can.

Recorded evidence blocks (14)

What did Telmisartan's largest trial (1165781 people) and its longest (19 years) measure?


1165781 people in Telmisartan's largest registered study, 19 years in its longest registered window, measuring ONTARGET. 3-fold Composite Endpoint of Doubling of Serum Creatinine, Progression to End Stage Renal Disease (ESRD) and All-cause Mortality in Diabetic Nephropathy Patients. ClinicalTrials.gov · 2026-09-01

50 phase4, 39 phase1, 39 phase3, 35 na or unstated, 23 phase2, 11 na, 1 early phase1; NCT07652567; 2026-04-30. Last human test completed 2026, NCT07652567.

Interpretation These counts include studies where Telmisartan was a comparison treatment, a background treatment or an exposure in an observational study, and the longest window may be a planned end date. Trial roles have not yet been classified for this record.

Show the evidence
  • phase4
    50
  • phase1
    39
  • phase3
    39
  • na or unstated
    35
  • phase2
    23
  • na
    11
2 more recorded rows
  • early phase1
    1
  • Last recorded human test NCT07652567
    2026-04-30

recorded 2026-09-01 · last checked 2026-09-04

From mouse to human: where has Telmisartan shown lifespan?


mouse: mechanism-only, rat: mechanism-only and human: lifespan (193): the rungs where Telmisartan has a recorded finding. Europe PMC and ClinicalTrials.gov · organism ladder · 2026-09-01

ONTARGET. 3-fold Composite Endpoint of Doubling of Serum Creatinine, Progression to End Stage Renal Disease (ESRD) and All-cause Mortality in Diabetic… — the recorded outcome words.

Yeast C. elegans Drosophila Mouse mechanism-onlyRat mechanism-onlyDog Non-human primate Human lifespan
Show the evidence
  • mouse
    mechanism-only
  • rat
    mechanism-only
  • human NCT00153101
    lifespan; ONTARGET. 3-fold Composite Endpoint of Doubling of Serum Creatinine, Progression to End Stage Renal Disease (ESRD) and All-cause Mortality in Diabetic Nephropathy Patients; 193

recorded 2026-09-01 · last checked 2026-09-04

15 of Telmisartan's trials stopped: futility/efficacy, accrual/recruitment, funding/business, other?


futility/efficacy (2), accrual/recruitment (6), funding/business (1) and other (6): Telmisartan's stop wording, clustered. ClinicalTrials.gov · 2026-09-01

"Primary investigator moved to different university"; 15 of 193 registered studies

Show the evidence

Trial

  • NCT00185705
    terminated; "Primary investigator moved to different university"
  • NCT00559286
    terminated; "logistic reasons, patients could not be recruited"
  • NCT00863980
    terminated; "Principle investigator resigned in 2013"
  • NCT01202721
    terminated; "Terminated early due to lack of study feasibility and poor patient recruitment"
  • NCT02085265
    terminated; "Lack of recruitment."
  • NCT02338232
    terminated; "Lack of Accrual"
9 further recorded trials
  • NCT02968160
    terminated; "Due to poor enrollment rate"
  • NCT03504566
    withdrawn; "Registered and published incorrectly"
  • NCT03868839
    terminated; "Lack of funding"
  • NCT04021550
    withdrawn; "Covid-19 Pandemic prevented this study from beginning"
  • NCT04359953
    terminated; "difficulty in recruiting"
  • NCT04360551
    terminated; "Decrease in COVID-19 cases locally"
  • NCT04606563
    terminated; "DSMC recommendation due to futility"
  • NCT04715763
    terminated; "Poor recruitment due to decrease in COVID-19 rates locally"
  • NCT06483789
    suspended; "Recruitment paused for Data Monitoring Committee (DMC) to review interim analysis data."

recorded 2026-09-01 · last checked 2026-09-04

Human studies of Telmisartan used Telmisartan 40 mg/HCTZ 12.5 mg — over how long?


studies of Telmisartan used the recorded amount. ClinicalTrials.gov · 2026-09-01

20 recorded entries; human; capsule; also "Telmisartan 40 mg/HCTZ 12.5 mg", "Telmisartan 40 mg", "Telmisartan capsule 40 mg"

Show the evidence

human

  • NCT00144222
    Telmisartan 40 mg/HCTZ 12.5 mg
  • NCT00144222
    Telmisartan 40 mg
  • NCT00153088
    capsule; Telmisartan capsule 40 mg
  • NCT00153088
    capsule; Telmisartan capsule 80 mg
  • NCT00274144
    telmisartan 40 mg
  • NCT00281580
    Telmisartan 20 mg
14 more recorded rows
  • human NCT00281580
    Telmisartan 80 mg
  • human NCT00326768
    Telmisartan 80 mg/HCTZ 12.5 mg
  • human NCT00421863
    Micardis 80 mg
  • human NCT00863980
    Micardis Tablets 40mg
  • human NCT01050062
    Telmisartan 80mg
  • human NCT01050062
    Telmisartan 40mg
  • human NCT01202721
    Micardis 40/80 mg
  • human NCT01286558
    40 mg telmisartan
  • human NCT01286558
    80 mg telmisartan
  • human NCT01356017
    Telmisartan 80mg, S-amlodipine 5mg
  • human NCT01356017
    Micardis 80mg, Anydipine S 5mg
  • human NCT01356017
    Micardis 80mg
  • human NCT02087540
    Placebo(for Telmisartan 80mg)
  • human NCT02231788
    Telmisartan/S-Amlodipine 40/2.5mg

recorded 2026-09-01 · last checked 2026-09-04

Telmisartan's half-life is 24 hours — which schedules were studied?


24 hours, the half-life Telmisartan's label states. openfda-label · 57da6ef2-2e86-4e4d-90df-73a2a8cf97f6 · 2026-08-30

bioavailability 42% %.

Show the evidence
  • half life
    24 hours hours; Telmisartan shows bi-exponential decay kinetics with a terminal elimination half-life of approximately 24 hours.
  • bioavailability
    42% %; At 40 mg and 160 mg, the bioavailability was 42% and 58%, respectively.
  • metabolism
    Metabolism and Elimination Following either intravenous or oral administration of 14 C-labeled telmisartan, most of the administered dose (>97%) was eliminated unchanged in feces via biliary excretion; only minute amounts were found in the urine (0.91% and 0.49% of total radioactivity, respectively).

recorded 2026-08-30 · last checked 2026-09-04

Which of 24 h mean diastolic blood pressure, 24 h mean systolic blood pressure and after one year of treatment in proteinuria did Telmisartan's trials measure?


24 h mean diastolic blood pressure, 24 h mean systolic blood pressure and after one year of treatment in proteinuria lead 40 outcome terms across Telmisartan's trials. ClinicalTrials.gov · 2026-09-01

glomerular filtration rate gfr after five years of treatment, at 8 weeks in seated trough cuff mean dbp, seated trough cuff mean dbp, study a annual change in total kidney volume, home blood pressure in the early morning and incidence of adverse events follow.

Show the evidence
  • supine diastolic blood pressure at trough
    1
  • first recurrent stroke of any type fatal or nonfatal
    1
  • after one year of treatment in proteinuria
    1
  • glomerular filtration rate gfr after five years of treatment
    1
  • at 8 weeks in seated trough cuff mean dbp
    1
  • seated trough cuff mean dbp
    1
14 more recorded rows
  • study a annual change in total kidney volume
    1
  • home blood pressure in the early morning
    1
  • incidence of adverse events
    1
  • changes in electrocardiogram
    1
  • homa index
    1
  • blood pressure surge in the morning
    1
  • blood pressure
    1
  • metabolic profiles including lipid profile and blood glucose
    1
  • il 6
    1
  • high sensitivity c reactive protein
    1
  • trough seated systolic blood pressure at week 8
    1
  • efficacy
    1
  • seated trough cuff systolic blood pressure to week 7
    1
  • control of blood pressure and decline in triglycerides level
    1

recorded 2026-09-01 · last checked 2026-09-04

Which of Telmisartan's 8 ongoing trials reports first?


8 registered trials of Telmisartan are open; earliest completion 2027-02. ClinicalTrials.gov · 2026-09-01

All-cause mortality; Tolerability of oral telmisartan; latest 2033-03-01

Show the evidence

Trial

  • NCT02735707
    "Randomized, Embedded, Multifactorial Adaptive Platform Trial for Community- Acquired Pneumonia"; n 20000; "All-cause mortality"; 2028-02
  • NCT06168487
    "Telmisartan in Prostate Cancer"; n 36; "Tolerability of oral telmisartan"; 2027-04-01
  • NCT06815497
    "Telmisartan in Combination With Cytotoxic Regimens in Platinum-Resistant Ovarian Cancer"; n 33; "Progression free survival"; 2029-05-14
  • NCT07207057
    "Edmond J. Safra Accelerating Clinical Trials in Parkinson's Disease: A Multiarm Multi-stage Platform Trial"; n 1200; "Movement Disorder Society-Sponsored Revision of the Unified Parkinson's Disease Rating Scale (MDS-UPDRS) Parts I and II combined"; 2031-07-31
  • NCT07370506
    "Telmisartan for Prevention of Doxorubicin-Induced Cardiotoxicity in Breast Cancer Patients"; n 36; "Change in Left Ventricular Ejection Fraction (LVEF)"; 2027-02
  • NCT07547878
    "Rapid and Simultaneous Initiation of Four Guideline-Directed CKD Therapies (RAPID-CKD)"; n 64; "On-study retention rate at 6 months"; 2029-03-31
2 further recorded trials
  • NCT07568574
    "Impact of Medically Supervised Performance-Enhancing Substances (PES) on Elite Athletes"; n 60; "The incidence and severity of Treatment-related adverse events (TRAEs), including adverse events (AEs) and serious adverse events (SAEs), as assessed by the study physicians from baseline to 5.5 years after enrollment."; 2033-03-01
  • NCT07784608
    "A Clinical Trial to Evaluate the Drug-drug Interactions of Co-administered 'HUC2-744-A' and 'HUC2-744-B' in Healthy Adult Volunteers"; n 28; "AUCτ"; 2027-11

recorded 2026-09-01 · last checked 2026-09-04

Which running trial of Telmisartan could settle lifespan?


NCT02735707 measures All-cause mortality, reading out 2028-02.

2 open trials; n 20000; "Randomized, Embedded, Multifactorial Adaptive Platform Trial for Community- Acquired Pneumonia"

Show the evidence

Trial

  • NCT02735707
    "Randomized, Embedded, Multifactorial Adaptive Platform Trial for Community- Acquired Pneumonia"; n 20000; "All-cause mortality"; 2028-02
  • NCT06815497
    "Telmisartan in Combination With Cytotoxic Regimens in Platinum-Resistant Ovarian Cancer"; n 33; "Progression free survival"; 2029-05-14

Which 62 trials of Telmisartan posted no result?


Posted no result
62 of 62 completed trials
Registrations
NCT00274612, NCT00274118, NCT00274144, NCT00240422, NCT00153049 and NCT00490958, and 56 more
Completion dates
oldest 2003-11; newest 2023-06-30
Show the evidence

Trial

  • NCT00274612
    2003-11
  • NCT00274118
    2004-01
  • NCT00274144
    2004-05
  • NCT00240422
    2004-07
  • NCT00153049
    2005-06
  • NCT00490958
    2005-06
14 further recorded trials
  • NCT00144222
    2005-08
  • NCT00153088
    2005-11
  • NCT00153023
    2005-12
  • NCT00407862
    2006-06
  • NCT00257491
    2006-08
  • NCT00146341
    2006-09
  • NCT00316095
    2007-08
  • NCT00326768
    2007-08
  • NCT00926341
    2008-09
  • NCT00421863
    2009-01
  • NCT00538486
    2009-06
  • NCT00750113
    2009-08
  • NCT00560430
    2009-10
  • NCT00452192
    2009-12

At the median, Telmisartan's trials enrolled 180 people — anything larger?


Median enrolment
180
Largest enrolment
1165781
Registered trials counted
193

What do 1568 spontaneous reports say about Telmisartan — and not say?


These are reports people sent to a regulator. They do not show the medicine caused the reaction. Nobody counted how many people took the medicine and reported nothing. The same event can be reported more than once, and many reports are incomplete. News coverage, lawsuits and new warnings change how often people report. A count is not a rate and not a risk.

Telmisartan appears in spontaneous reports to regulators. Across the 10 most-reported reaction terms, 1568 reaction mentions were counted: hypotension 233; hyponatraemia 219; acute kidney injury 168; hypertension 165. open-targets-adr · CHEMBL1017 · 2026-06-24

Show the evidence
  • hypotension
    233
  • hyponatraemia
    219
  • acute kidney injury
    168
  • hypertension
    165
  • blood pressure increased
    162
  • hyperkalaemia
    159
4 more recorded rows
  • loss of consciousness
    129
  • renal failure acute
    129
  • renal failure
    111
  • suicide attempt
    93

recorded 2026-06-24 · last checked 2026-09-04

Telmisartan and CYP2C19: shared by which compounds?


CYP2C19 appear in Telmisartan's recorded interaction sentences, 2 in all. openfda-label+europepmc · 2026-08-30

Interpretation pharmacokinetics

Show the evidence

CYP2C19

  • pharmacokinetics
    Telmisartan is not expected to interact with drugs that inhibit cytochrome P450 enzymes; it is also not expected to interact with drugs metabolized by cytochrome P450 enzymes, except for possible inhibition of the metabolism of drugs metabolized by CYP2C19.
  • pharmacokinetics
    Telmisartan is not metabolized by the cytochrome P450 system and had no effects in vitro on cytochrome P450 enzymes, except for some inhibition of CYP2C19.

recorded 2026-08-30 · last checked 2026-09-04

Was Telmisartan studied with fasting and exercise?


fasting and exercise are named in Telmisartan's label sentences: "There were no significant differences between the two groups in week 12 changes for HOMA-IR or fasting triglycerides (- 0.18 ± 1.24 vs 0.39 ± 1.39, p = 0.181; - 26 ± 76 vs - 10 ± 81 mg/dL, p = 0.679, respectively) (telmisartan vs placebo)." openfda-label+europepmc · 2026-08-30

2 recorded statements; fasting, exercise

Show the evidence
  • fasting
    There were no significant differences between the two groups in week 12 changes for HOMA-IR or fasting triglycerides (- 0.18 ± 1.24 vs 0.39 ± 1.39, p = 0.181; - 26 ± 76 vs - 10 ± 81 mg/dL, p = 0.679, respectively) (telmisartan vs placebo).
  • exercise
    In people with peripheral artery disease (PAD), the Telmisartan Plus Exercise to Improve Functioning in Peripheral Artery Disease (TELEX) randomized clinical trial tested whether telmisartan (TEL), with or without exercise, significantly improved 6-minute walk distance at 6-month follow-up, compared with placebo (PLA).

recorded 2026-08-30 · last checked 2026-09-04

What is recorded about Telmisartan and AMPK?


"This study aimed to delineate the cardioprotective mechanisms of low-dose Telmisartan against myocardial ischemia/reperfusion (I/R) injury, specifically by distinguishing between AMPK-dependent and AMPK-independent pathways using AMPK kinase-dead (KD) mouse models." — where Telmisartan and AMPK appear together. Europe PMC · pathway abstract search · 2026-03-19

AMPK, autophagy, mTOR, sirtuin, NAD+; PMID 41864588, 40935114, 32893519, 38783939

Show the evidence

AMPK

  • PMID 41864588
    "This study aimed to delineate the cardioprotective mechanisms of low-dose Telmisartan against myocardial ischemia/reperfusion (I/R) injury, specifically by distinguishing between AMPK-dependent and AMPK-independent pathways using AMPK kinase-dead (KD) mouse models."
  • PMID 41864588
    "Consistently, Telmisartan activated AMPK, phosphorylated cTnI(Ser150), PGC-1α, and increased the Bcl-2/Bax ratio in WT but not KD mice, whereas LKB1 activation occurred independently of AMPK."
  • PMID 41864588
    "Low-dose Telmisartan confers cardioprotection against I/R injury via dual mechanisms: it primarily utilizes AMPK-dependent signaling to combat oxidative stress, apoptosis, and infarction, while independently of AMPK, it preserves calcium homeostasis and activates LKB1."
  • autophagy PMID 40935114
    "Key targets included Signal Transducer and Activator of Transcription 3 (STAT3), B-cell lymphoma 2 (Bcl2), and Nuclear Factor kappa-light-chain-enhancer of activated B cells (NF-κB), regulators of cellular autophagy, suggesting telmisartan's potential interaction with autophagy-related pathways."

mTOR

  • PMID 32893519
    "Telmisartan decreased VSMC proliferation, which was accompanied by decreased phosphorylations of mammalian target of rapamycin (mTOR) at Ser2448 (p-mTOR-Ser<sup>2448</sup>) and p70 S6 kinase (p70S6K) at Thr389 (p-p70S6K-Thr<sup>389</sup>) in dose- and time-dependent manners."
  • PMID 32893519
    "Co-treatment with compound C, a specific AMPK inhibitor, or ectopic expression of the dn-AMPKα1 gene, significantly reversed telmisartan-inhibited VSMC proliferation, p-mTOR-Ser<sup>2448</sup> and p-p70S6K-Thr<sup>389</sup> levels."
  • PMID 32893519
    "Finally, telmisartan also exhibited inhibitory effects on VSMC proliferation by increasing p-AMPK-Thr<sup>172</sup> and decreasing p-mTOR-Ser<sup>2448</sup> and p-p70S6K-Thr<sup>389</sup> in a PDGF-induced in vitro atherosclerosis model."

autophagy

  • PMID 38783939
    "The findings suggest the protective efficiency of telmisartan and nano Sp extract against cardiotoxicity via activations of the antioxidant, antiapoptotic, and autophagy signaling pathways."
  • PMID 25249228
    "In conclusion, this study provides evidence that the chronic pharmacological activation of the PPARγ-mediated autophagy pathway using telmisartan may represent a promising therapeutic strategy for atherosclerosis."
  • sirtuin PMID 23137106
    "Telmisartan has been reported to function as a partial agonist of the peroxisome proliferator-activated receptor (PPAR) γ, which is also targeted by the nicotinamide adenine dinucleotide (NAD)-dependent deacetylase (SIRT1)."
  • NAD+ PMID 23137106
    "Telmisartan has been reported to function as a partial agonist of the peroxisome proliferator-activated receptor (PPAR) γ, which is also targeted by the nicotinamide adenine dinucleotide (NAD)-dependent deacetylase (SIRT1)."
  • sirtuin PMID 23137106
    "Our results indicate that telmisartan acts through a PPARγ-independent pathway, but at least partially exerts its effects by acting directly on skeletal muscle AMPK/SIRT1 pathways."

NAD+

  • PMID 22890154
    "Conversely, cotreatment with telmisartan inhibited both NAD(P)H oxidase activity and production of ROS."
  • PMID 22890154
    "These findings suggest that glomerular injury resulting from FK506 is caused by oxidative stress mediated by activation of NAD(P)H oxidase and that telmisartan exerts a renoprotective effect via antioxidative activity."

recorded 2026-03-19 · last checked 2026-09-04

Where it is registered
Identifiers, relations and other names

The exact record

ChEMBL id
CHEMBL1017
PubChem CID
65999
CAS number
144701-48-4
RxCUI
73494
InChIKey
RMMXLENWKUUMAY-UHFFFAOYSA-N
Development code
BIBR-277, BIBR 277 SE, C09CA07
Also called
Bibr-277se, Kinzalmono, Pritor, Semintra, Telmisartan actavis, Telmisartan teva, angiotensin receptor blocker, arb, bay68-9291, ckd-828, gliosartan, kinzal
Trade name
Micardis, Telmisartan component of kinzalkomb, Telmisartan component of micardis hct, Telmisartan component of micardisplus, Telmisartan component of onduarp, Telmisartan component of pritorplus, Telmisartan component of tolucombi, Telmisartan component of twynsta, Telmisartan teva pharma, Tolura, KINZALKOMB COMPONENT TELMISARTAN, MICARDISPLUS COMPONENT TELMISARTAN
Salt form
tah tablet
Sources (11)

Sources

  • ClinicalTrials.gov clinicaltrials.gov ·
  • ClinicalTrials.gov ClinicalTrials.gov API v2 snapshot 2026-09-01T09:00:05 ·
  • this record's own fields 2,3,5 ·
  • Europe PMC dose-response search ·
  • Europe PMC pathway abstract search ·
  • Europe PMC search ·
5 more sources

ChEMBL ATC CC BY-SA · ClinicalTrials.gov — US Government work · Europe PMC — metadata only, under the recorded legal gate · Open Targets 26.06 — CC0 · derived from this page's own recorded fields; no external licence · mixed register set; per-register licences in docs/specs/corpus-20k-sources.md · openFDA / DailyMed — US Government work

How these records are assembled · Which registers were checked

Index-quality checks
  • identity passed: no open identity hold
  • required summary fields resolved: 5 required field(s) not terminal: Why people use it, Best-supported result, Most important common problem, Biggest unanswered question, Human evidence
  • public claims reviewed: 0 reviewed claim(s); drafts are never rendered
  • source coverage passed: 11 source rows
  • no critical contamination: no quarantine open
  • canonical metadata passed: slug and display name present
  • no raw internal fields: enforced by the copy-contract test over the rendered page

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