Last reviewed 2026-05-29 · How we verify

Relaxine dosage

Hospices Civils de Lyon · Phase 2 active Biologic ✓ Verified May 2026

Relaxine dosage is a Biologic drug developed by Hospices Civils de Lyon. It is currently in Phase 2 development.

Relaxin is being studied in clinical trials for conditions such as infertility and embryo transfer, with dosage as the intervention. However, there is no information available on the specific dosage of relaxin in these studies or its mechanism of action, as its modality is listed as "Unknown" in ChEMBL.

Likelihood of approval

15.3% vs 15.3% industry baseline

If approved by FDA: likely 2031–2034

Steps remaining: Phase 3 → NDA/BLA submission

Confidence: Medium

Why this estimate

Baseline phase 2 → approval rate +15.3pp
Industry-wide phase 2 drugs reach approval ~15.3% of the time (BIO/Informa 2023 industry benchmark across all therapeutic areas).

Predicted approval windows by jurisdiction (conditional on FDA approval)

Regulator	Country	Likely year	Lag vs FDA
FDA	US	2031–2034	—
EMA	EU	2032–2035	+0.7 yr
MHRA	GB	2032–2035	+0.7 yr
Health Canada	CA	2032–2036	+0.9 yr
TGA	AU	2032–2036	+1.2 yr
PMDA	JP	2032–2036	+1.5 yr
NMPA	CN	2033–2037	+2.3 yr
MFDS	KR	2032–2036	+1.4 yr
CDSCO	IN	2032–2037	+1.8 yr
ANVISA	BR	2033–2037	+2.3 yr

Hover any row for the lag rationale. Lag estimates are reduced when the drug has FDA Breakthrough or EMA PRIME designation (sponsors file globally in parallel).

Estimate based on the BIO/Informa industry phase transition rates plus per-drug modifiers for therapeutic area, sponsor type, FDA designations, mechanism, and trial design. Per-jurisdiction lags from Tufts CSDD international approval studies. Not investment, clinical or regulatory advice. Methodology: /methodology#likelihood.

At a glance

Generic name	Relaxine dosage
Sponsor	Hospices Civils de Lyon
Modality	Biologic
Phase	Phase 2

Approved indications

No approved indications tracked.

Common side effects

No common side effects on file.

Key clinical trials

Plasma Relaxin Measurement Based on Endometrial Preparation for Embryo Transfer

Primary sources

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

Source	Used for
ClinicalTrials.gov	Trial 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:

Relaxine dosage CI brief — competitive landscape report
Relaxine dosage updates RSS · CI watch RSS
Hospices Civils de Lyon portfolio CI

Frequently asked questions about Relaxine dosage

What is Relaxine dosage?

Relaxine dosage is a Biologic drug developed by Hospices Civils de Lyon.

Who makes Relaxine dosage?

Relaxine dosage is developed by Hospices Civils de Lyon (see full Hospices Civils de Lyon pipeline at /company/hospices-civils-de-lyon).

What development phase is Relaxine dosage in?

Relaxine dosage is in Phase 2.

Manufacturer: Hospices Civils de Lyon — full pipeline

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