Last update 28 Feb 2026

ALY-688

Overview

Basic Info

Drug Type
Synthetic peptide
Synonyms
DAsn-Ile-Pro-Nva-Leu-Tyr-DSer-Phe-Ala-DSer, ADP 355, ADP-355
+ [5]
Action
agonists
Mechanism
Adiponectin receptors agonists
Inactive Indication
Originator Organization
Inactive Organization-
License Organization-
Drug Highest PhasePhase 1
First Approval Date-
RegulationOrphan Drug (United States)
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Structure/Sequence

Molecular FormulaC53H80N12O14
InChIKeyFAOICIJDRRZKCE-UBKMUEJXSA-N
CAS Registry1793835-62-7

R&D Status

10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
Dry Eye SyndromesPhase 3
United States
19 May 2021
Metabolic Dysfunction Associated SteatohepatitisPhase 1
Bulgaria
31 Mar 2026
ObesityPhase 1
Australia
19 May 2021
Muscular Dystrophy, DuchennePreclinical
United States
19 Feb 2024
Primary Biliary CholangitisPreclinical
United States
19 Feb 2024
Pulmonary FibrosisPreclinical
United States
19 Feb 2024
Scleroderma, SystemicPreclinical
United States
19 Feb 2024
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date
Phase 1/2
138
hpsuhrcfyl(fgxhoknpns) = dlaegdoglz tggjffnpah (lpabqpjnva, 2.34)
-
23 Apr 2023
Vehicle
hpsuhrcfyl(fgxhoknpns) = rfzeboquop tggjffnpah (lpabqpjnva, 2.25)
Phase 1/2
138
hlmpuiptnt(mirasewvyq) = with no adverse systemic effects. hhrpewpxzn (vplkxfaonn )
Positive
01 Dec 2022
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Translational Medicine

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Deal

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Core Patent

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Clinical Trial

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Approval

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Biosimilar

Competitive landscape of biosimilars in different countries/locations. Phase 1/2 is incorporated into phase 2, and phase 2/3 is incorporated into phase 3.
Competitive landscape of biosimilars in different countries/locations. Phase 1/2 is incorporated into phase 2, and phase 2/3 is incorporated into phase 3.

Regulation

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