Is serelaxin FDA-approved?

No. Serelaxin isn't FDA-approved, and Drugs@FDA lists no application with it as an active ingredient.

Checked 1 Nov 2026. The sources are below.

Serelaxin

Also: RLX030, recombinant human relaxin-2

Status label in the Peptimes Library
Not FDA-Approved
Routes in Peptimes
Other
Updated
1 Nov 2026

US regulatory status

  • FDA status

    Not FDA-Approved. Drugs@FDA lists no application with serelaxin as an active ingredient.

    Source: Drugs@FDA, checked 1 Nov 2026

How to track it in Peptimes

Add serelaxin in My Protocols and set the schedule you already follow: days of the week, times of day and a start date. Peptimes never suggests an amount when you log or schedule a dose. Its Library entry shows the status label “Not FDA-Approved”.

  • Logging: the amount you took and how you feel. It’s logged with the route Other, so there’s no injection site to record.
  • Reminders and history: reminders at your times, Dose History, the Calendar and CSV or JSON export work as described on the peptide tracker app page.

Peptimes is a tracking app, not medical advice. Talk to a licensed clinician about your treatment. Peptimes doesn’t sell serelaxin or any other compound.

More sources

  • FDA, Global Substance Registration System, Serelaxin, checked 1 Nov 2026: its two chains, the names RLX030 and recombinant human relaxin, and an EMA assessment code recording that the EU refused it as Reasanz for heart failure.
  • NIH, ClinicalTrials.gov, studies of serelaxin, checked 1 Nov 2026: registered studies, all completed or ended early.
  • FDA, Drugs@FDA, checked 1 Nov 2026: no application lists serelaxin as an active ingredient.

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