Tesamorelin

Tesamorelin is a synthetic stabilized analog of GHRH composed of the full 44-amino acid sequence of GHRH, conjugated with a trans-3-hexenoic acid modification t...

FDA-approved (Egrifta) for HIV-associated lipodystrophy. Active research ongoing

AOD-9604

AOD-9604 is a modified peptide fragment corresponding to amino acids 176-191 from the C-terminal region of human growth hormone, with a stabilizing tyrosine mod...

Has completed Phase I/II human safety trials with acceptable tolerability. Incon

Fragment 176-191

Fragment 176-191 refers to the unmodified C-terminal peptide fragment of human growth hormone spanning amino acids 176-191. It is the precursor compound from wh...

Primarily preclinical data. Less studied than AOD-9604. Research-grade compound

Kisspeptin

Kisspeptin refers to a family of peptides (KP-54, KP-14, KP-13, KP-10) encoded by the KISS1 gene, which are essential regulators of the hypothalamic-pituitary-g...

Active Phase II clinical trials for infertility and reproductive disorders. A sy

Follistatin-344

Follistatin-344 is a 344-amino acid isoform of the native glycoprotein follistatin, engineered for targeted research applications. Follistatin is a potent endog...

Active clinical trials as gene therapy (AAV1-FS344) for neuromuscular diseases i

MOTS-c

MOTS-c is a 16-amino acid mitochondrial-derived peptide (MDP) encoded by a short open reading frame within the 12S rRNA gene of mitochondrial DNA. It is one of ...

Preclinical data primarily in mice and cell culture. Growing human observational

5-Amino-1MQ

5-Amino-1MQ is a small-molecule methylquinolinium derivative that functions as a selective inhibitor of nicotinamide N-methyltransferase (NNMT), an enzyme that ...

Preclinical only (cell culture and mouse models). Growing clinical interest. No

Semaglutide

Semaglutide is an FDA-approved synthetic 31-amino acid analog of glucagon-like peptide-1 (GLP-1), modified with a C18 fatty acid chain via a linker to albumin f...

FDA-approved for T2D, obesity, and cardiovascular risk reduction. Active researc

Tirzepatide

Tirzepatide is an FDA-approved first-in-class dual GIP/GLP-1 receptor agonist peptide that simultaneously activates both glucose-dependent insulinotropic polype...

FDA-approved (2022 T2D, 2023 obesity). Active Phase III research in NASH, heart

Retatrutide

Retatrutide is an investigational first-in-class triple agonist targeting GLP-1, GIP, and glucagon receptors simultaneously. Developed by Eli Lilly, it has demo...

Phase III trials ongoing (7 additional Phase III readouts expected in 2026). Not

Liraglutide

Liraglutide is an FDA-approved GLP-1 receptor agonist peptide with 97% structural homology to human GLP-1, modified with a fatty acid side chain enabling self-a...

FDA-approved (2010 T2D, 2014 obesity). Extensive post-marketing safety data. Pri

Cagrilintide

Cagrilintide is a long-acting acylated amylin analog developed by Novo Nordisk. Amylin is a 37-amino acid peptide co-secreted with insulin from pancreatic beta ...

Phase III clinical trials ongoing (CagriSema for obesity and T2D). Phase II data

Pramlintide

Pramlintide (brand name Symlin) is a synthetic 37-amino acid analog of human amylin with three proline substitutions that prevent the spontaneous aggregation an...

FDA-approved 2005 for T1D and T2D as insulin adjunct. Long-term safety data avai

Glucagon

Glucagon is a 29-amino acid pancreatic peptide hormone secreted by alpha cells of the islets of Langerhans in response to hypoglycemia. Its primary function is ...

FDA-approved for emergency hypoglycemia (1960). GCGR agonism as a component of c

Insulin (Endogenous Peptide)

Insulin is a 51-amino acid peptide hormone produced by pancreatic beta cells, consisting of an A-chain (21 AA) and B-chain (30 AA) connected by two disulfide bo...

FDA-approved since 1982 (recombinant human insulin). Multiple analog formulation

Ghrelin

Ghrelin is a 28-amino acid acylated peptide hormone produced primarily by X/A-like cells of the gastric fundus. It is the endogenous ligand for the growth hormo...

Characterized 1999 (Kojima et al.). Not used therapeutically as exogenous ghreli

Cholecystokinin (CCK)

Cholecystokinin (CCK) is a peptide hormone found in multiple forms (CCK-8, CCK-33, CCK-58) secreted by enteroendocrine I-cells of the duodenum and jejunum in re...

Extensively characterized endogenous peptide. CCK analogs and CCK-1R agonists un

PYY (Peptide YY)

Peptide YY (PYY) is a 36-amino acid gut peptide released from L-cells of the distal intestine and colon in proportion to caloric intake. The truncated form PYY(...

Endogenous peptide: extensively characterized. PYY(3-36) intranasal (NN9748): Ph

Exendin-4 (Exenatide)

Exendin-4 is a 39-amino acid peptide originally isolated from the venom of the Gila monster lizard (Heloderma suspectum) that shares 53% sequence homology with ...

FDA-approved 2005 (Byetta, twice-daily). Extended-release formulation Bydureon (

Survodutide

Survodutide (BI 456906) is an investigational dual agonist of GLP-1 (glucagon-like peptide-1) and glucagon receptors, developed by Boehringer Ingelheim. Unlike ...

Phase II trials completed for obesity and NASH (2023-2024). Phase III trials ini

Cardarine (GW-501516)

Cardarine (GW-501516) is a PPARδ (peroxisome proliferator-activated receptor delta) agonist, not a SARM in the strict sense, but it is commonly grouped with SAR...

Clinical development discontinued by GSK in 2007 due to carcinogenicity in roden

BRP (BRINP2-Related Peptide)

BRP (BRINP2-Related Peptide) is a naturally occurring 12-amino acid peptide discovered in 2025 by Stanford researchers led by Dr. Katrin Svensson using an AI al...

Research ongoing

Amycretin

Amycretin is a novel, unimolecular long-acting dual agonist of both the GLP-1 and amylin receptors, developed by Novo Nordisk as a next-generation obesity and t...

Research ongoing

Orforglipron

Orforglipron (brand name Foundayo, formerly LY3502970) is a first-in-class oral, non-peptide, small-molecule GLP-1 receptor agonist developed by Eli Lilly (orig...

Research ongoing

MariTide (maridebart cafraglutide)

MariTide (maridebart cafraglutide, formerly AMG 133) is a novel bispecific antibody-peptide conjugate developed by Amgen, engineered to simultaneously antagoniz...

Research ongoing

Pemvidutide

Pemvidutide (ALT-801) is a once-weekly, balanced 1:1 GLP-1/glucagon dual receptor agonist developed by Altimmune, Inc. (Nasdaq: ALT), distinguished by its equal...

Research ongoing

Mazdutide

Mazdutide (IBI362, marketed as Xinermei in China) is the world's first approved dual glucagon (GCG)/GLP-1 receptor agonist, developed by Innovent Biologics unde...

Research ongoing

CagriSema

CagriSema is an investigational fixed-dose combination of two distinct obesity medications in a single once-weekly subcutaneous injection: cagrilintide 2.4 mg (...

Research ongoing

Dulaglutide

Dulaglutide is a long-acting glucagon-like peptide-1 (GLP-1) receptor agonist marketed by Eli Lilly under the brand name Trulicity. Approved by the FDA in Septe...

FDA-approved 2014 for T2D, label expanded 2020 to include MACE reduction. Active

Avexitide

Avexitide is an investigational, first-in-class glucagon-like peptide-1 (GLP-1) receptor antagonist derived from exendin(9-39), a 31-amino-acid truncated fragme...

Investigational. Phase 3 LUCIDITY trial enrollment complete (March 2026); toplin

EB618 (Oral Oxyntomodulin Tablet)

EB618 is an oral tablet formulation of oxyntomodulin (OXM) being developed by Entera Bio for metabolic and fibrotic conditions, including obesity, type 2 diabet...

Preclinical. NHP pharmacokinetic data submitted to ENDO 2026.

GEP-44 (Chimeric GLP-1/Y1/Y2 Multi-Agonist)

GEP-44 is a 44-amino-acid chimeric peptide developed in the laboratory of Robert Doyle at Syracuse University, in collaboration with the Blevins/Roth groups at ...

Preclinical. Published rodent and shrew efficacy and mechanism data from 2021–20

HL4 (Macrocyclic Insulin Receptor Agonist)

HL4 is a 19-residue cyclic peptide that activates the human insulin receptor (IR) on intact cells. It was reported on March 12, 2026 in Angewandte Chemie Intern...

Preclinical, cell-based only. The published work characterizes binding, activati

Danuglipron (Pfizer Discontinued Oral GLP-1)

Danuglipron is a non-peptide small-molecule GLP-1 receptor agonist that Pfizer advanced through clinical development for obesity and type 2 diabetes before disc...

Development discontinued by Pfizer in April 2025 after a hepatic adverse event i

DA-1726

DA-1726 is an investigational oxyntomodulin-analogue peptide developed by MetaVia Inc. (Nasdaq: MTVA) as a once-weekly subcutaneous dual agonist at the glucagon...

Phase 1 active. Phase 1 Part 3a/3b titration studies ongoing as of May 2026; lon