readthroughSign in
Jul 17, 2026Weekly roundup

Lilly posts results for five completed Phase 1 studies, opens three new early trials

Results this week cover orforglipron, LY3502970 and pegilodecakin, while three new Phase 1 studies for MORF-057, eloralintide and LY4178256 begin recruiting.

Eli Lilly posted results for five completed early-stage studies and registered three new Phase 1 trials this week.

  • Orforglipron was tested against carbamazepine in a Phase 1 drug interaction study in healthy participants, assessing carbamazepine's effect on orforglipron blood levels and clearance, and safety when the two drugs were given alone or together.1 No participants in the combination arm on Day 15 had serious adverse events (0/28).1
  • A Phase 1 bioequivalence study comparing orforglipron capsules and tablets in participants with obesity or overweight completed on June 2, 2025, with results posted July 17, 2026.2 The study enrolled 533 participants.2
  • A Phase 1 dose-titration study of LY3502970 in Chinese participants with obesity or overweight and weight-related comorbidities gave the drug or placebo orally and completed with results posted.3 Enrollment was 24 participants.3
  • A Phase 1 single- and multiple-ascending dose study of LY3502970 in Japanese participants with type 2 diabetes evaluated side effects of the drug.4 The study enrolled 62 participants.4
  • A completed crossover study compared pharmacokinetics of pegilodecakin delivered by pre-filled syringe versus vial in healthy adults.5 ARMO BioSciences is listed as a collaborator alongside lead sponsor Eli Lilly.
  • A new Phase 1 study of LY4268989 (MORF-057) is recruiting healthy participants to compare two tablet formulations under different meal conditions.6 Enrollment is estimated at 50 participants.6
  • A new Phase 1 open-label study is recruiting healthy participants to evaluate pharmacokinetics, safety and tolerability of two eloralintide solution formulations.7 Enrollment is estimated at 58 participants.7
  • A new Phase 1 placebo-controlled single- and multiple-ascending dose study of LY4178256 is recruiting healthy participants to assess safety and tolerability.8 Enrollment is estimated at 88 participants.8

Written by readthrough’s AI from the linked primary sources and fact-checked against them automatically before publishing. Not investment advice.