Asset profile

survodutide

Peptide

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Reliablesignal

Evidence outlook · lead readout

SYNCHRONIZE-1 (NCT06066515) · Obesity

The completed lead evidence has the design features that historically survive confirmatory trials: randomized, controlled, and adequately powered against a prespecified clinically accepted endpoint.

SYNCHRONIZE-1 (NCT06066515): In this randomized, double-blind, placebo-controlled Phase 3 trial in 726 adults with obesity, survodutide produced substantially greater weight loss than placebo at 76 weeks (average 16.6% body weight reduction vs 3.2% with placebo, a highly significant difference).

Caveat: this result is taken from a company announcement or a news report of one, not from the trial registry or a peer-reviewed publication. Treat the figures as the sponsor's own statement, not as independently verified evidence.

Also in development:Type 2 Diabetes · Phase 3MASH / NASH · Phase 3

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Competitive landscape

144 competitors in this universe: 6 direct rivals (same mechanism and indication), 0 same-class, 138 same-indication; 40 further along in development.

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DrugStageModalityMechanismEvidence signalReported efficacygraded featured trials
Survodutide: this drugPhase 3PeptideGLP-1/glucagon receptor (dual)
MazdutidePhase 3PeptideGLP-1/glucagon receptor (dual)
PemvidutidePhase 3PeptideGLP-1/glucagon receptor (dual)
AZD9550Phase 2PeptideGLP-1/glucagon receptor (dual)
OPK-88006Phase 1/2—GLP-1/glucagon receptor (dual)
PB-718Phase 1/2PeptideGLP-1/glucagon receptor (dual)
DA-1726Phase 1PeptideGLP-1/glucagon receptor (dual)
AfrezzaApprovedPeptideInsulin receptor (basal), Insulin
Alogliptin (Nesina)ApprovedSmall moleculeDPP-4
Bexagliflozin (Brenzavvy)ApprovedSmall moleculeSGLT2
Canagliflozin (Invokana)ApprovedSmall moleculeSGLT2
Dapagliflozin (Farxiga / Forxiga)ApprovedSmall moleculeSGLT2
Dulaglutide (Trulicity)ApprovedPeptideGLP-1 receptor
Empagliflozin (Jardiance)ApprovedSmall moleculeSGLT2
Ertugliflozin (Steglatro)ApprovedSmall moleculeSGLT2
Glipizide (Glucotrol)ApprovedSmall moleculeSulfonylurea receptor (SUR1)

…and 129 more. Research shows the complete landscape.

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Research adds each competitor's evidence grade and sourced trial results, aligned per race, so you can see who actually has the data.

Upcoming events

(11 total)

Estimated primary-completion dates from ClinicalTrials.gov. These are registry estimates, never confirmed readout dates; they can move as trials progress.

2026 (1)
December 2026 (1)
Phase 1ObesityRecruiting
Est. primary completion 2026-12-08 · NCT07768813 · CT.gov ↗
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2027 (4)
January 2027 (3)
Phase 1ObesityActive not recruiting
Est. primary completion 2027-01-06 · NCT05202353 · CT.gov ↗
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Phase 1ObesityActive not recruiting
Est. primary completion 2027-01-08 · NCT06745284 · CT.gov ↗
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Phase 1ObesityActive not recruiting
Est. primary completion 2027-01-26 · NCT07407348 · CT.gov ↗
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November 2027 (1)
Phase 2Chronic Kidney DiseaseNot yet recruiting
Est. primary completion 2027-11-30 · NCT07206290 · CT.gov ↗
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2028 (3)
January 2028 (1)
Phase 3Type 2 DiabetesRecruiting
Est. primary completion 2028-01-17 · NCT07754461 · CT.gov ↗
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June 2028 (1)
Phase 3ObesityNot yet recruiting
Est. primary completion 2028-06-25 · NCT07855900 · CT.gov ↗
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July 2028 (1)
Phase 3ObesityNot yet recruiting
Est. primary completion 2028-07-26 · NCT07850050 · CT.gov ↗
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2029 (2)
April 2029 (1)
Phase 3MASH / NASHNot yet recruiting
Est. primary completion 2029-04-29 · NCT07850063 · CT.gov ↗
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June 2029 (1)
Phase 3MASH / NASHRecruiting
Est. primary completion 2029-06-05 · NCT06632457 · CT.gov ↗
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2031 (1)
December 2031 (1)
Phase 3MASH / NASHRecruiting
Est. primary completion 2031-12-27 · NCT06632444 · CT.gov ↗
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See the full readout calendar ↗

All registered studies

Every ClinicalTrials.gov study of this drug's own program, grouped by indication and phase. Research unlocks the studies themselves: titles, statuses, dates and featured-trial cross-links.

Phase 3 (12)
Phase 2 (4)
Phase 1 (20)