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Fat loss

Survodutide

Boehringer Ingelheim's GLP-1/glucagon dual agonist in Phase 3, showing 17-22% weight loss with a cardiovascular outcomes trial underway.

Investigational (Phase 3) Fat loss Longevity

Reviewed 2026-09-12
Full name
BI 456906 (dual glucagon and GLP-1 receptor agonist)
Also known as
BI 456906, GLP-1/GCGR dual agonist
Regulatory status
Investigational (Phase 3) | Cardiovascular outcomes trial ongoing

Origin

Developed by Boehringer Ingelheim as a once-weekly subcutaneous GLP-1/glucagon receptor dual agonist. In Phase 3 following positive Phase 2 dose-finding trials in obesity, with multiple regional Phase 3 trials active including a dedicated cardiovascular outcomes trial.

Mechanism

Selective dual agonist of GLP-1R and GCGR with balanced activity at both, combining appetite suppression with hepatic lipogenesis inhibition and higher energy expenditure. Preclinical and early clinical data suggest it preferentially reduces visceral and hepatic adiposity.

Research summary

Evidence

Phase 2/3 data show survodutide 3.6-4.8 mg produces 17-22% body weight reductions over 52 weeks, with reported liver-fat reductions of 60-80% in some cohorts. Heart-rate elevation is observed and under formal cardiovascular evaluation. GI adverse events are dose-limiting but typically mild-to-moderate. Evidence is limited to 52-76 weeks of exposure.

Evidence tier: Investigational (Phase 3) — see the methodology note for how this is assessed.

Citations

Reported benefits

  • weight loss (17-22% body weight reduction)
  • improved glycemic control
  • preferential visceral and liver-fat reduction
  • potential cardioprotection (under investigation)

Dosing protocols reported in the literature & community

These are protocols reported by compounding pharmacies, published trials, or self-experimentation communities — not a prescription. Start low, especially for anything new.

Reported dosing protocols
RouteReported protocol
Subcutaneous injectionOnce-weekly: gradual escalation to maintenance at 3.6 or 4.8 mg over 4-8 weeks.

Side effects

  • nausea
  • vomiting
  • diarrhea
  • constipation
  • fatigue
  • increased heart rate
  • potential QTc prolongation (under investigation)

Safety notes

Safety: GI tolerability improves with slower dose escalation. Heart-rate elevation is consistent across dual agonists and under formal evaluation. Cardiovascular outcomes and safety remain the key open Phase 3 question.
Community & reddit notes (anecdotal — not clinical evidence)

Biohacker access is limited since it's a Phase 3 drug. Scattered anecdotal trial-participant reports suggest efficacy similar to or better than mazdutide with slightly better liver-fat reduction.

Mixing compatibility

Pulled from a community-charted mixing-compatibility reference (anecdotal, clinic-use, and community-reported signals) — not a safety guarantee. Verify independently before combining anything.

Note: This chart's source flags GLP-1/GIP/glucagon-receptor drugs as broadly avoided in combination with other research peptides across the board — not a peptide-specific interaction, more a general caution against stacking incretin drugs with anything else. Treat any combination here as unverified.