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A First-in-Human Study to Assess the Safety, Pharmacokinetics, and Pharmacodynamics of HMB-003 in Healthy Volunteers
RecruitingPhase 1Healthy volunteers welcome
Who can join
Ages 18 to 50 · All sexes · Healthy volunteers welcome
Full eligibility criteria
Inclusion Criteria: * Participant is aged 18 to 50 years, inclusive, at the time of signing informed consent. * Overall healthy as determined by medical evaluation including physical examination, vital signs, laboratory tests, and ECG. Exclusion Criteria: * Participant has a history of clinically significant hypersensitivity to any excipients of the study drug * Participant is pregnant, breastfeeding, or \<6 weeks postpartum. * Participant has received investigational drug or device in another clinical study within 30 days or 5 half-lives, whichever is longer, before dosing.
About the study
The purposes of this clinical study are
1. To see how the new drug (HMB-003) under study is tolerated in healthy volunteers, and if there are any important side effects. 2. To measure the amount of HMB-003 in the body after injection.
What is being tested
- HMB-003 (drug)
- Placebo (drug)
Sponsor: Hemab ApS · Participants: 40 · Started: Aug 17, 2026
Contact the study team
- Clinical Trials · Phone: 001 888 493 8148
Official record on ClinicalTrials.gov — NCT07798505
Locations in the U.S.
| Texas | Worldwide Clinical Trials, San Antonio |
From ClinicalTrials.gov, data retrieved Oct 2, 2026. Each study sets its own eligibility; the study team decides who can join.