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Vonoprazan 20 mg

Rehman Medical Institute - RMI · FDA-approved active Small molecule Quality 2/100

Vonoprazan 20 mg is a Small molecule drug developed by Rehman Medical Institute - RMI. It is currently FDA-approved. Also known as: Potassium-competitive acid blocker, TAK-438, Takecab, vocinti.

Vonoprazan 20 mg, marketed by Rehman Medical Institute (RMI), is a drug with a key composition patent expiring in 2028. The drug's market position and primary indication are not specified, but it holds a significant competitive advantage due to its patent protection until 2028. The primary risk is the potential increase in competition post-patent expiry in 2028.

At a glance

Generic nameVonoprazan 20 mg
Also known asPotassium-competitive acid blocker, TAK-438, Takecab, vocinti
SponsorRehman Medical Institute - RMI
ModalitySmall molecule
PhaseFDA-approved

Approved indications

No approved indications tracked.

Common side effects

No common side effects on file.

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:

Frequently asked questions about Vonoprazan 20 mg

What is Vonoprazan 20 mg?

Vonoprazan 20 mg is a Small molecule drug developed by Rehman Medical Institute - RMI.

Who makes Vonoprazan 20 mg?

Vonoprazan 20 mg is developed and marketed by Rehman Medical Institute - RMI (see full Rehman Medical Institute - RMI pipeline at /company/rehman-medical-institute-rmi).

Is Vonoprazan 20 mg also known as anything else?

Vonoprazan 20 mg is also known as Potassium-competitive acid blocker, TAK-438, Takecab, vocinti.

What development phase is Vonoprazan 20 mg in?

Vonoprazan 20 mg is FDA-approved (marketed).

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