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MECASERMIN RINFABATE

Insmed · FDA-approved approved Recombinant protein Quality 17/100

MECASERMIN RINFABATE is a Recombinant protein drug developed by Insmed. It is currently FDA-approved (first approved 2005) for Laron-type isolated somatotropin defect.

At a glance

Generic nameMECASERMIN RINFABATE
SponsorInsmed
ModalityRecombinant protein
Therapeutic areaOther
PhaseFDA-approved
First approval2005

Approved indications

Common side effects

No common side effects on file.

Key clinical trials

Patents

PatentExpiryType
Biologic Exclusivity

Primary sources

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

SourceUsed for
FDA labelMechanism, indications, dosing, boxed warnings, drug interactions
ClinicalTrials.govTrial enrolment, design, endpoints, results
FDA Orange BookPatents + exclusivity

Competitive intelligence

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Frequently asked questions about MECASERMIN RINFABATE

What is MECASERMIN RINFABATE?

MECASERMIN RINFABATE is a Recombinant protein drug developed by Insmed, indicated for Laron-type isolated somatotropin defect.

What is MECASERMIN RINFABATE used for?

MECASERMIN RINFABATE is indicated for Laron-type isolated somatotropin defect.

Who makes MECASERMIN RINFABATE?

MECASERMIN RINFABATE is developed and marketed by Insmed (see full Insmed pipeline at /company/insmed).

When was MECASERMIN RINFABATE approved?

MECASERMIN RINFABATE was first approved on 2005.

What development phase is MECASERMIN RINFABATE in?

MECASERMIN RINFABATE is FDA-approved (marketed).

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing