A Study to Evaluate ALN-4915 in Adult Healthy Volunteers
Recruiting now · Phase 1 · Has a placebo group
Conditions studied: Healthy Volunteers
In brief
The purpose of this study is to evaluate the safety, tolerability, pharmacodynamics (PD) and pharmacokinetics (PK) of ALN-4915.
Key facts
- Study ID
- NCT07535606
- Run by
- Alnylam Pharmaceuticals
- People needed
- 44
- Starts
- 2026-03-02
- Expected to finish
- 2027-07-31
- Last updated by the study team
- 2026-07-23
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Is willing and able to complete all study assessments
You may not qualify if…
- Has alanine aminotransferase (ALT) or aspartate aminotransferase (AST) >upper limit of normal (ULN)
- Has total bilirubin >ULN
- Has no history of invasive infection by an encapsulated organism
- Has no known complement or immunologic deficiency
Where it is running
- Clinical Trial Site — London, United Kingdom (enrolling)
Full record on ClinicalTrials.gov
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