A Study to Learn How Different Amounts of the Study Medicine Called PF-07985631 Are Tolerated and Act in the Body in Healthy Adults
NCT07235150 · Status: RECRUITING · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 76
Last updated 2026-03-19
Summary
The purpose of this study is to learn about the safety and effects of the study medicine (called PF-07985631) for the possible treatment of a kidney disease called IgA nephropathy.
This study is seeking participants who
* are male or female between 18 and 45 years of age (55 for Japanese/Chinese/multiple dose participants)
* are deemed to be healthy Participants in this study will receive PF-07985631 or placebo. A placebo does not have any medicine in it but looks just like the medicine being studied.
PF-07985631 or placebo will be given as a small needle injection (in the abdomen, thigh or back of the arm) at the study clinic. Most participants will receive PF-07985631 or placebo one time. Some participants may receive PF-07985631 or placebo twice.
The study will compare the experiences of people receiving PF-07985631 to those of the people who do not. This will help decide if PF-07985631 is safe and effective.
Participants who take PF-07985631 or placebo will take part in this study for about four- four and a half months. During this time, they will stay at the study clinic for 12 to 19 days and will have 7 more study visits at the study clinic.
During study clinic stays and study visits, blood samples will be done and safety reviews completed.
Conditions
- Healthy
Interventions
- DRUG
-
PF-07985631
Experimental Pfizer compound which will be SC
- DRUG
-
Placebo which will be SC
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Pfizer CT.gov Call Center · Pfizer
Study Design
- Allocation
- RANDOMIZED
- Purpose
- BASIC_SCIENCE
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 55 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2025-12-11
- Primary Completion
- 2027-08-24
- Completion
- 2027-08-24
Countries
- Australia
Study Locations
More Related Trials
-
A Study to Evaluate the Effectiveness and Safety of IONIS-FB-LRx, an Antisense Inhibitor of Complement Factor B, in Adult Participants With Primary IgA Nephropathy
NCT04014335 ·Status: COMPLETED ·Phase: PHASE2
-
The Effect of Nefecon® in Patients With Primary IgA Nephropathy at Risk of Developing End-stage Renal Disease
NCT01738035 ·Status: COMPLETED ·Phase: PHASE2
-
A Renal Impairment Study for PF-04965842
NCT03660241 ·Status: COMPLETED ·Phase: PHASE1
-
A Study to Learn How the Body Processes the Study Medicine Called PF-07923568 in People With Loss of Kidney Function
NCT06037031 ·Status: COMPLETED ·Phase: PHASE1
-
Single Dose Safety Study for Compound to Treat Anemia in Patients With Renal Impairment
NCT00935831 ·Status: COMPLETED ·Phase: PHASE1
-
Renal Impairment Study of PF-07321332 Boosted With Ritonavir in Adult Participants With Renal Impairment and in Healthy Participants With Normal Renal Function.
NCT04909853 ·Status: COMPLETED ·Phase: PHASE1
-
Study of the Safety and Efficacy of OMS721 in Patients With Immunoglobulin A (IgA) Nephropathy
NCT03608033 ·Status: TERMINATED ·Phase: PHASE3
-
A Study to Learn How Renal Impairment Affects the Pharmacokinetics of PF-07817883.
NCT06586216 ·Status: COMPLETED ·Phase: PHASE1
-
Study to Evaluate the Pharmacokinetics, Safety, and Pharmacodynamics of INCB054707 in Participants With Normal and Impaired Renal Function and Participants on Hemodialysis
NCT05624723 ·Status: COMPLETED ·Phase: PHASE1
-
PF-04634817 Renal Impairment Study
NCT01791855 ·Status: COMPLETED ·Phase: PHASE1
-
Renal Impairment Study of PF-06700841
NCT04260464 ·Status: COMPLETED ·Phase: PHASE1
-
Study of HRS-5965 in Healthy Subjects and Subjects With Renal Insufficiency
NCT05505955 ·Status: COMPLETED ·Phase: PHASE1
-
A Study of Mezagitamab in Adults With Primary Immunoglobulin A Nephropathy Receiving Stable Background Therapy
NCT05174221 ·Status: COMPLETED ·Phase: PHASE1
-
Study of Efficacy and Safety of LNP023 in Primary IgA Nephropathy Patients
NCT04578834 ·Status: COMPLETED ·Phase: PHASE3
-
Study on Efficacy and Safety of LNP023 in C3 Glomerulopathy Patients Transplanted and Not Transplanted
NCT03832114 ·Status: COMPLETED ·Phase: PHASE2
-
Study Assessing PK and Safety of MGTA-145 in Subjects With Normal Estimated GFR and Varying Degrees of Renal Impairment
NCT04154670 ·Status: COMPLETED ·Phase: PHASE1
-
A Study of the Safety, Tolerability, Pharmacokinetics and Efficacy of Treatment With AP1189 in Patients With iMN and Severe Proteinuria
NCT04456816 ·Status: RECRUITING ·Phase: PHASE2
-
A Study to Evaluate the Safety, Tolerability, and Effects on Blood and Urine Markers of Single Ascending Dose of GSK4771261 in Healthy Participants and Participants With Autosomal Dominant Polycystic Kidney Disease
NCT06734234 ·Status: RECRUITING ·Phase: PHASE1
-
A Study of Pharmacokinetics and Safety of LY3537031 in Participants With Normal Renal Function and Participants With Renal Impairment
NCT07165015 ·Status: COMPLETED ·Phase: PHASE1
-
Safety and Efficacy Study of OMS906 in Patients With C3G and ICGN
NCT06209736 ·Status: RECRUITING ·Phase: PHASE2
-
A Renal Impairment Study for PF-06651600
NCT04037865 ·Status: TERMINATED ·Phase: PHASE1
-
A Study of AEB1102 (Pegzilarginase) in Patients With Arginase I Deficiency
NCT03378531 ·Status: COMPLETED ·Phase: PHASE2
-
First-in-Human Study of BCX9930 in Healthy Volunteers and Patients With PNH
NCT04330534 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Efficacy of Immunosuppressive Therapy for IgA Nephropathy With Stage 3 or 4 CKD
NCT05510323 ·Status: RECRUITING ·Phase: PHASE3
-
A Study of Mezagitamab in Adults With Kidney Condition Called IgA Nephropathy
NCT06963827 ·Status: RECRUITING ·Phase: PHASE3