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NCT05841238
A Multiple Dose Study of LY3502970 in Healthy Overweight and Obese Participants
Phase 1 trial testing LY3502970 in Healthy in 52 participants. Completed in 13 November 2023.
14 September 2023
Quick facts
| Lead sponsor | Eli Lilly and Company |
|---|---|
| Phase | Phase 1 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | basic science |
| Enrollment | 52 |
| Start date | 26 April 2023 |
| Primary completion | 14 September 2023 |
| Estimated completion | 13 November 2023 |
| Sites | 3 locations across United States |
Drugs / interventions tested
- LY3502970 — full drug profile →
Conditions studied
Sponsor
Eli Lilly and Company — full company profile →
Who can join
Adults 18 to 70, any sex, with Healthy or Obese. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The main purpose of this study is to evaluate how much LY3502970 gets into the bloodstream and how long it takes the body to eliminate when administered orally as tablet and capsule formulations along with effect of food on LY3502970 in healthy overweight and obese participants. The study will also evaluate the safety and tolerability of LY3502970 in these participants. The study is conducted in two parts (part A and B) and will last up to 135 days including the screening period.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Pharmacokinetic Bioequivalence of Orforglipron Tablets and Capsules in Healthy Participants With Obesity or Overweight.
Ma X, Li YG, Raha S, Sperry DC, et al · · 2026 · PMID 41994902 · DOI 10.1111/dom.70783
Verify or expand the search:
- PubMed search for NCT05841238
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of LY3502970
Trials testing the same drug.
- NCT06085482 — A Phase I Study of LY3502970 in Healthy Participants · Phase 1 · completed
- NCT06023095 — A Study of LY3502970 in Chinese Participants With Obesity or Are Overweight With Weight-related Comorbidities · Phase 1 · completed
- NCT05936138 — A Study of LY3502970 in Participants With Normal and Impaired Renal Function · Phase 1 · completed
- NCT05882032 — A Study of LY3502970 in Participants With Impaired and Normal Liver Function · Phase 1 · completed
- NCT05573230 — A Drug Interaction Study of Cyclosporine and LY3502970 in Healthy Participants · Phase 1 · completed
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Currently open trials in the same condition.
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Other Eli Lilly and Company trials
Trials by the same sponsor.
- NCT07533006 — A Study of LY4005130 in Adult Participants With Severe Alopecia Areata (Hair Loss) · Phase 2 · not yet recruiting
- NCT07533019 — A Study of LY4005130 in Adult Participants With Non-Segmental Vitiligo · Phase 2 · not yet recruiting
- NCT07247357 — A Study of LY4064809 in Healthy Adult Chinese Participants · Phase 1 · completed
- NCT07124013 — A Study of Olomorasib (LY3537982) in Healthy Japanese Participants · Phase 1 · completed
- NCT07030127 — A Study of LY3985863 in Healthy Participants · Phase 1 · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT05841238 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 9 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Eli Lilly and Company
- Last refreshed: 2 October 2024
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05841238.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing