Clinical Trial

Study of the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Preliminary Efficacy of QLS2319 in Healthy Subjects and Cancer Cachexia

Not Yet Recruiting Phase 1/2
View on ClinicalTrials.gov →
Summary
Study To Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Preliminary Efficacy of QLS2319 in Healthy Subjects and Cancer Cachexia
Trial Details
NCT Number NCT07735104
Lead Sponsor Qilu Pharmaceutical Co., Ltd.
Conditions Cancer Cachexia Syndrome, Cancer Cachexia
Enrollment 88 participants
Start Date 2026-09-01
Primary Completion 2028-10-30 (estimated)
Study Completion 2028-12-31 (estimated)
Updated on ClinicalTrials.gov 2026-07-29