MedPath

Study to Evaluate the Safety, Tolerability and Pharmacokinetics of PF-04958242 in Healthy Adult Volunteers

Phase 1
Terminated
Conditions
Healthy Volunteers
Interventions
Drug: Placebo
Registration Number
NCT01238679
Lead Sponsor
Biogen
Brief Summary

The primary objective of this study evaluates the safety and tolerability of multiple, escalating doses of PF-04958242 administered orally to healthy adult participants.This study also evaluates the plasma and urine multiple dose pharmacokinetics (PK) of PF-04958242.

Detailed Description

A decision was made to terminate the B1701002 study so that emerging data from the study and from a preclinical study in rats could be further examined and incorporated into a new study design and protocol.

This study was previously posted by Pfizer, Inc. Sponsorship of the trial was transferred to Biogen.

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
20
Inclusion Criteria
  • Body Mass Index (BMI) of 17.5 to 30.5 kilograms per meter quared (kg/m2);
  • Total body weight >50 kilograms (kg) (110 pounds [lbs]);

Key

Exclusion Criteria
  • Evidence or history of clinically significant hematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric, neurologic, or allergic disease (including drug allergies, but excluding untreated, asymptomatic, seasonal allergies at time of dosing);
  • Positive urine drug screen;
  • Pregnant or nursing females, and females of child bearing potential;
  • Severe acute or chronic medical or psychiatric condition or laboratory abnormality that may increase the risk associated with study participation or investigational product administration or may interfere with the interpretation of study results and, in the judgment of the investigator, would make the participant inappropriate for entry into this study.

NOTE: Other protocol defined Inclusion/Exclusion criteria may apply

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Cohort 3PF-04958242Participants received an oral solution of 0.10 mg of PF-04958242, every 24 hours for 14 days.
Cohort 4PF-04958242Participants received an oral solution of 0.15 mg of PF-04958242, every 24 hours for 14 days.
Cohort 6PF-04958242Participants received an oral solution of 0.25 mg of PF-04958242, every 24 hours for 14 days.
Cohort 2PF-04958242Participants received an oral solution of 0.05 mg of PF-04958242, every 24 hours for 14 days.
Matching PlaceboPlaceboParticipants received an oral solution of matching placebo, every 12 or 24 hours for 14 days.
Cohort 1PF-04958242Participants received an oral solution of 0.03 milligrams (mg) of PF-04958242, every 12 hours for 14 days.
Cohort 5PF-04958242Participants received an oral solution of 0.20 mg of PF-04958242, every 24 hours for 14 days.
Primary Outcome Measures
NameTimeMethod
Time to Reach Maximum Plasma Concentration (Tmax) for Steady StateDay 1 and at multiple time points up to Day 17
Time to Reach Maximum Plasma Concentration (Tmax) for Single DoseDay 1 and at multiple time points up to Day 17
Apparent Total Clearance of the Drug from Plasma (CL/F) for Steady StateDay 1 and at multiple time points up to Day 17
Apparent Volume of Distribution During Terminal Phase (Vz/F) for Steady StateDay 1 and at multiple time points up to Day 17
Elimination Half-Life (t1/2) for Steady StateDay 1 and at multiple time points up to Day 17
Maximum Observed Plasma Concentration (Cmax) for Steady StateDay 1 and at multiple time points up to Day 17
Area Under the Plasma Drug Concentration-Time Curve During a Dosage Interval (AUCτ) for Steady StateDay 1 and at multiple time points up to Day 17
Accumulation Ratio (AUC(τ,ss)/AUC(τ,sd)) for Steady StateDay 1 and at multiple time points up to Day 17
Percent of Dose Eliminated in Urine Unchanged (Ae%)Day 14
Amount of PF-04958242 Eliminated in Urine Unchanged (Ae)Day 14
Number of Participants Experiencing Adverse Events and Serious Adverse EventsBaseline up to Day 23

An adverse event is any untoward medical occurrence in a clinical investigation subject administered a product or medical device. A serious adverse event or serious adverse drug reaction is any untoward medical occurrence at any dose that: Results in death; Is life-threatening (immediate risk of death); Requires inpatient hospitalization or prolongation of existing hospitalization; Results in persistent or significant disability/incapacity; Results in congenital anomaly/birth defect.

Maximum Plasma Drug Concentration (Cmax) for Single DoseDay 1 and at multiple time points up to Day 17
Area Under the Concentration Time-curve During a Dosage Interval (AUCτ) for Single DoseDay 1 and at multiple time points up to Day 17
Renal Clearance (CLr)Day 14
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Research Site

🇸🇬

Singapore, Singapore

© Copyright 2025. All Rights Reserved by MedPath