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Survodutide with Tesamorelin

Mechanism-tag overlap and published literature for Survodutide and Tesamorelin, pulled verbatim from each Kalios compound profile. Kalios is a literature reference, not a recommendation.

Mechanism overlap

Mechanism tags are verbatim labels on each compound's profile. Generic tags ("peptide", "small-molecule", "research-chemical") are excluded from this overlap view. Tags are descriptive — not an inference about combined effect.

SURVODUTIDE TESAMORELIN 1 UNIQUE TAGS 2 UNIQUE TAGS 0 SHARED
Survodutide unique glucagon-glp-1-receptor-dual-agonist
Shared none
Tesamorelin unique fda-approved-ghrh-analogvisceral-adiposity

Co-administration notes from the literature

Verbatim summary text pulled from each compound's profile data. Researchers studying Survodutide and Tesamorelin have published these mechanism-level observations. Not a co-administration recommendation.

Evidence level: mechanistic only

GHRH analog for visceral adiposity — FDA-approved in HIV-associated lipodystrophy. Mechanistically orthogonal to survodutide's GLP-1/glucagon action. Theoretical pairing for adiposity-focused metabolic optimization; no controlled combination data.

Quick facts

Survodutide

RouteSubQ once weekly
Half-life~6 days (weekly dosing)
FDA statusNot approved; Phase 3
WADANot specifically listed
Full Survodutide profile →

Tesamorelin

RouteSubQ once daily
Half-life~26 min (SC)
FDA statusApproved (2010)
WADANot listed
Full Tesamorelin profile →

Literature table

Classified references from each compound profile. Click a column header to sort. Click a PMID to open PubMed. Findings are quoted verbatim from each profile's literature_summary; nothing here is added or interpreted.

Year Compound Source Finding
2024SurvodutideWharton S, le Roux CW, Kosiborod MN, et al. Survodutide for treatment of obesity: rationale and design of two randomized phase 3 clinical trials (SYNCHRONIZE-1 and -2). Obesity (Silver Spring). 2024.human trial, Phase 3
2023SurvodutideBoehringer Ingelheim. Phase III studies — survodutide in obesity and overweight. Boehringer Ingelheim corporate press release and investor materials, 2023–2025.human trial, Phase 3
2025SurvodutideLe Roux CW, et al. Survodutide, a glucagon receptor/glucagon-like peptide-1 receptor dual agonist, improves blood pressure in adults with obesity: A post hoc analysis from a randomized, placebo-controlled, dose-finding, phase 2 trial. Diabetes Obes Metab. 2025. doi:10.1111/dom.1…human trial, Phase 2
2024SurvodutideLe Roux CW, Steen O, Lucas KJ, Startseva E, Unseld A, Hennige AM. Glucagon and GLP-1 receptor dual agonist survodutide for obesity: a randomised, double-blind, placebo-controlled, dose-finding phase 2 trial. Lancet Diabetes Endocrinol. 2024;12(3):162-173. doi:10.1016/S2213-8587(…human trial, Phase 2
2024SurvodutideSanyal AJ, Bedossa P, Fraessdorf M, Neff GW, Lawitz E, Bugianesi E, Anstee QM, Hussain SA, Martins EB, Walker M, Oldham P, Starova B, Ogawa W, Wong VW, Ratziu V, Younes R, Hosseini-Tabatabaei A, Loomba R. A Phase 2 Randomized Trial of Survodutide in MASH and Fibrosis. N Engl J M… PMID 38847460human trial, Phase 2
2023SurvodutideJastreboff AM, Kaplan LM, Frías JP, Wu Q, Du Y, Gurbuz S, Coskun T, Haupt A, Milicevic Z, Hartman ML; Retatrutide Phase 2 Obesity Trial Investigators. Triple-Hormone-Receptor Agonist Retatrutide for Obesity — A Phase 2 Trial. N Engl J Med. 2023;389(6):514-526. PMID: 37366315. (F… PMID 37366315human trial, Phase 2
SurvodutideClinicalTrials.gov. NCT04667377 (Phase 2 obesity); NCT04771273 (Phase 2 MASH, study 1404-0043); NCT06066879 (SYNCHRONIZE-1); NCT06066892 (SYNCHRONIZE-2).human trial, Phase 2
2023SurvodutideJungnik A, Arrubla Martinez J, Plum-Mörschel L, Kapitza C, Lamers D, Thamer C, Unseld A, Hennige AM. Phase I studies of the safety, tolerability, pharmacokinetics and pharmacodynamics of the dual glucagon receptor/glucagon-like peptide-1 receptor agonist BI 456906. Diabetes Obes…human trial, Phase 1
2016SurvodutideTschöp MH, Finan B, Clemmensen C, Gelfanov V, Perez-Tilve D, Müller TD, DiMarchi RD. Unimolecular polypharmacy for treatment of diabetes and obesity. Cell Metab. 2016;24(1):51-62. PMID: 27411008. (Foundational review on multi-receptor agonism rationale including GLP-1/glucagon.) PMID 27411008human study
2022SurvodutideZimmermann T, Thomas L, Baader-Pagler T, Haebel P, Simon E, Reindl W, Bajrami B, Rist W, Uphues I, Drucker DJ, Klein H, Santhanam R, Hennige AM, Hamilton B, Hennig R, Dux M, Hamprecht B, Bierwisch D, Neubauer H, Tschank G, Stengelin S, Redemann N, Wiedenmann A, Pagler T, et al.…preclinical, in vivo
2024SurvodutideLoomba R, Hartman ML, Sanyal AJ. Two Trials of Therapeutics for MASH with Liver Fibrosis. Reply. N Engl J Med. 2024;391(15):1462-1463. PMID: 39413388. PMID 39413388research article
2024SurvodutidePolyzos SA. Two Trials of Therapeutics for MASH with Liver Fibrosis. N Engl J Med. 2024;391(15):1461. PMID: 39413385. PMID 39413385research article
2010TesamorelinFalutz J, Mamputu JC, Potvin D, Moyle G, Soulban G, Loughrey H, et al. Effects of tesamorelin (TH9507), a growth hormone-releasing factor analog, in human immunodeficiency virus-infected patients with excess abdominal fat: a pooled analysis of two multicenter, double-blind place… PMID 20101189human trial, Phase 3
TesamorelinClinicalTrials.gov. NCT00123253, NCT00435136 (Phase 3 registration); NCT01263717 (JAMA liver fat); NCT02196831 (Lancet HIV NAFLD); NCT00675506 (Arch Neurol cognition).human trial, Phase 3
2019TesamorelinStanley TL, Fourman LT, Feldpausch MN, Purdy J, Zheng I, Pan CS, et al. Effects of tesamorelin on non-alcoholic fatty liver disease in HIV: a randomised, double-blind, multicentre trial. Lancet HIV. 2019;6(12):e821-e830. PMID: 31611038. PMID 31611038human trial
2014TesamorelinStanley TL, Feldpausch MN, Oh J, Branch KL, Lee H, Torriani M, Grinspoon SK. Effect of tesamorelin on visceral fat and liver fat in HIV-infected patients with abdominal fat accumulation: a randomized clinical trial. JAMA. 2014;312(4):380-389. PMID: 25038357. PMID 25038357human trial
2005TesamorelinFalutz J, Allas S, Kotler D, Thompson M, Koutkia P, Albu J, et al. A placebo-controlled, dose-ranging study of a growth hormone releasing factor in HIV-infected patients with abdominal fat accumulation. AIDS. 2005;19(12):1279-1287. PMID: 16052083. PMID 16052083human trial
2004TesamorelinKoutkia P, Canavan B, Breu J, Torriani M, Kissko J, Grinspoon S. Growth hormone-releasing hormone in HIV-infected men with lipodystrophy: a randomized, controlled trial. JAMA. 2004;292(2):210-218. PMID: 15249570. PMID 15249570human trial
2012TesamorelinBaker LD, Barsness SM, Borson S, Merriam GR, Friedman SD, Craft S, Vitiello MV. Effects of growth hormone-releasing hormone on cognitive function in adults with mild cognitive impairment and healthy older adults: results of a controlled trial. Arch Neurol. 2012;69(11):1420-1429.… PMID 22869065human study
2011TesamorelinStanley TL, Falutz J, Mamputu JC, Soulban G, Potvin D, Grinspoon SK. Effects of tesamorelin on inflammatory markers in HIV patients with excess abdominal fat: relationship with visceral adipose reduction. Clin Infect Dis. 2011;53(11):1150-1158. PMID: 22016502. PMID 22016502human study
2008TesamorelinFalutz J, Allas S, Mamputu JC, Potvin D, Kotler D, Somero M, et al. Long-term safety and effects of tesamorelin, a growth hormone-releasing factor analogue, in HIV patients with abdominal fat accumulation. AIDS. 2008;22(14):1719-1728. PMID: 18690162. PMID 18690162human study
2007TesamorelinFalutz J, Allas S, Blot K, Potvin D, Kotler D, Somero M, et al. Metabolic effects of a growth hormone-releasing factor in patients with HIV. N Engl J Med. 2007;357(23):2359-2370. PMID: 18057338. PMID 18057338human study
2011TesamorelinDhillon S. Tesamorelin: a review of its use in the management of HIV-associated lipodystrophy. Drugs. 2011;71(8):1071-1091. PMID: 21668043. PMID 21668043review
2026TesamorelinWorld Anti-Doping Agency. The 2026 Prohibited List. Section S2 — Peptide Hormones, Growth Factors, Related Substances and Mimetics. wada-ama.org.regulatory / registry

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Frequently asked

Have Survodutide and Tesamorelin been studied together?

Researchers have published mechanistic-level co-administration discussion of Survodutide and Tesamorelin. No human co-administration trials are catalogued in the Kalios profiles. The pair page lists each compound's classified literature; full citations sit on each individual profile.

What mechanisms do Survodutide and Tesamorelin share?

Survodutide and Tesamorelin do not share a specific mechanism tag on their Kalios profiles. They appear on the same pair page because at least one profile lists the other in its co-administration data.

What is the FDA status of Survodutide and Tesamorelin?

Survodutide: Not approved; Phase 3. Tesamorelin: Approved (2010). FDA-status text is pulled verbatim from each compound profile. See /fda-pcac-2026.html for the broader FDA Pharmacy Compounding Advisory Committee context.

Where can I find the full research on Survodutide and Tesamorelin?

Full citation lists, dosing tables from the literature, reconstitution data, and the FDA / WADA status are on the individual compound profiles: the Survodutide profile and the Tesamorelin profile. The Kalios Stack Research Tool hub lists every compound covered.

Last updated: April 2026