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Recruiting Phase 1 NCT07535606

A Study to Evaluate ALN-4915 in Adult Healthy Volunteers

Phase 1 – testing safety in a small group of people
Conditions: Healthy Volunteers

Sponsor: Alnylam Pharmaceuticals

trial.available_in: БГ
Overview
The purpose of this study is to evaluate the safety, tolerability, pharmacodynamics (PD) and pharmacokinetics (PK) of ALN-4915.
Who can participate
Inclusion Criteria: * Is willing and able to complete all study assessments Exclusion Criteria: * 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
Interventions
ALN-4915
DRUG
Placebo
DRUG
Locations 1
United Kingdom (1)
Clinical Trial Site
London
Technical details
Status
Recruiting
Phase
Phase 1
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
18 Years
Maximum age
65 Years
Healthy volunteers
No
Start date
02.03.2026
Completion date
31.07.2027
Registry ID
NCT07535606
Source
clinicaltrials.gov
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