A Study to Learn About the Single Dose Pharmacokinetics of Study Medicine Called Tilrekimig in Healthy Adults When Co-Mixed With rHuPH20
Part of paid clinical trials in New Haven, Connecticut.
- Sponsor
- Pfizer
- Study ID
- NCT07792941
- Phase
- PHASE1
- Status
- Recruiting
Conditions
- Healthy
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 65 Years
- Healthy Volunteers
- Accepted
Interventions
- tilrekimig and rHuPH20 — DRUGsubcutaneous injection
Study Details
This study aims to learn how the body handles tilrekimig when given with another medicine called recombinant human hyaluronidase PH20 (rHuPH20). rHuPH20 is approved to help some medicines be taken up by the body when they are given together as an injection (shot) under the skin.
Key Dates
- First listed
- Aug 28, 2026
- Start date
- Aug 27, 2026
- Status verified
- Sep 2026
- Primary completion
- Feb 11, 2027
- Completion
- Feb 11, 2027
Study Design
- Enrollment
- 12 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- BASIC_SCIENCE
Arms
- Experimental: tilrekimig and rHuPH20a single dose of co-mixed tilrekimig and rHuPH20
Primary Outcome Measure
Tilrekimig area under the serum concentration-time curve from time zero to infinity (AUCinf) [ Time Frame: pre-dose, hours 12, 24, 48, 72, and 96 hours post dose. Days 8, 15, 30, 45, 60, 90, 120, and 150 post -dose ]
Central Contacts
- Pfizer CT.gov Call Center1-800-718-1021
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| New Haven Pfizer Clinical Research Unit (NH PCRU) | New Haven | Connecticut | 06511 | - |
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