U.S., Oct. 8 -- ClinicalTrials.gov registry received information related to the study (NCT07864311) titled 'A Phase 1 Study of VELA-101 in Adult Participants' on Oct. 02.
Brief Summary: This is a first-in-human (FIH), multicenter, randomized, double-blind, placebo-controlled study evaluating the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of VELA-101, following single-ascending doses via subcutaneous (SC) administration.
Study Start Date: Nov., 2026
Study Type: INTERVENTIONAL
Condition:
Healthy Participants
Hyperlipidemia
Intervention:
DRUG: VELA-101
subcutaneous injection
DRUG: Placebo
subcutaneous injection
Recruitment Status: NOT_YET_RECRUITING
Sponsor: Ursa Medicines
Disclaimer: Curated by HT Synd...