Clinical Pipeline

Bimagrumab

BYM338

Bimagrumab is a clinical-stage asset. Trial status and sponsor-reported findings remain time-sensitive and indication-specific.

Compare
EvidenceTier 2
RegulatoryInvestigational
SafetyUncertain or Concerning
Clinical phasePhase 2 evidence base
01

Overview

ClassActivin type II receptor antibody
Sponsor / developerClinical-stage developer
Review statusReviewed
Record IDPEP-032
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Plain-language guide

What it was designed or studied for

Designed for research into Body-composition research, Muscle-wasting research, Obesity research. It remains investigational for these uses.

How it works, simply

It tries to reduce biological signals that normally limit muscle growth. Whether that produces useful strength or function depends on the individual asset and evidence.

This simplified explanation is educational context, not a treatment recommendation or a substitute for the clinical evidence below.
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Clinical mechanism

Blocks activin type II receptor signaling, including pathways that restrain muscle growth.

Mechanism plausibility is not the same as demonstrated clinical benefit.
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Applications

  • Body-composition research
  • Muscle-wasting research
  • Obesity research
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Human evidence

Early or mid-stage human data exist, but confirmation, replication or long-term follow-up remains incomplete.

Tier 2
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Preclinical evidence

Mechanistic and preclinical findings are tracked separately and are not treated as proof of human clinical benefit.

MAP

Muscle & recovery profile

Each signal is scored independently from 0–5. There is no composite “best” score.

Growth relevance4/5
Preservation relevance4/5
Recovery relevance1/5
Mitochondrial support1/5
Connective tissue1/5
Human-data depth3/5
Safety confidence2/5
Evidence–hype gap2/5

Evidence classes

  • Phase 2 human evidence

What has been studied

  • Human studies have examined body composition, including lean-mass measures.

What is not established

  • Clinical benefit, durability and an approved muscle indication are not established.

Studied populations

  • Adults with obesity
  • People with muscle-wasting conditions in clinical research

Major limitations

  • Muscle-specific outcomes may be secondary, exploratory or absent from available studies.
  • Findings from one population, formulation or indication should not be generalized to another.

Evidence-source categories: primary regulatory record, clinical trial registry, peer reviewed literature. These editorial source categories require record-level primary links before publication-grade citation export.

06

Regulatory status

Investigational. Regulatory status is product- and jurisdiction-specific and does not automatically follow from an evidence score.

07

Safety

Uncertain or Concerning

  • Adverse effects vary by product and indication
  • Contraindications and interactions require label review
08

Interactions

Review the current product label and indication-specific literature for pharmacologic and absorption interactions.

09

Treatment pattern

Treatment patterns are product-, indication- and clinician-specific; this educational profile does not provide dosing guidance.

10

Manufacturing and quality

Approved-product identity, formulation and quality controls must not be extrapolated to compounded or RUO copies.

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Sources

  1. 01
    Primary regulatory record

    Source record prepared for primary-reference linking in the Supabase-backed editorial workflow.

  2. 02
    Clinical trial registry

    Source record prepared for primary-reference linking in the Supabase-backed editorial workflow.

  3. 03
    Peer-reviewed literature

    Source record prepared for primary-reference linking in the Supabase-backed editorial workflow.

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Gaps and unverified claims

  • Long-term outcomes and real-world safety are not yet established.
  • Current phase and catalysts require primary-source confirmation.
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Last reviewed

August 5, 2026 · Reviewed