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Trial record 1 of 1 for:    PF-06755347
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A First in HumanTrial to Evaluate The Safety, Tolerability, And Pharmacokinetics Of PF-06755347

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ClinicalTrials.gov Identifier: NCT03275740
Recruitment Status : Recruiting
First Posted : September 8, 2017
Last Update Posted : March 21, 2019
Sponsor:
Information provided by (Responsible Party):
Pfizer

Brief Summary:
This phase 1 single ascending dose study will provide a first in human assessment of safety and tolerability of PF-06755347 in healthy adult subjects. The pharmacokinetics and pharmacodynamics will also be evaluated.

Condition or disease Intervention/treatment Phase
Polyradiculoneuropathy, Chronic Inflammatory Demyelinating Idiopathic Thrombocytopenic Purpura Drug: PF-06755347 Drug: Placebo comparator Phase 1

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 64 participants
Allocation: Randomized
Intervention Model: Sequential Assignment
Intervention Model Description: single ascending dose study
Masking: Double (Participant, Investigator)
Masking Description: Double blind (investigator and subject), sponsor open
Primary Purpose: Treatment
Official Title: A PHASE 1, RANDOMIZED, DOUBLE-BLIND, SPONSOR-OPEN, PLACEBO-CONTROLLED, FIRST-IN-HUMAN TRIAL TO EVALUATE THE SAFETY, TOLERABILITY, AND PHARMACOKINETICS OF PF-06755347 AFTER SINGLE ASCENDING INTRAVENOUS INFUSIONS TO HEALTHY ADULT MALE PARTICIPANTS
Actual Study Start Date : December 20, 2018
Estimated Primary Completion Date : May 27, 2021
Estimated Study Completion Date : May 27, 2021


Arm Intervention/treatment
Experimental: PF-06755347 Drug: PF-06755347
Single doses of PF-06755347 will be administered, at planned dose levels of 0.01 mg/kg, 0.03 mg/kg, 0.1 mg/kg, 0.3 mg/kg, 1 mg/kg, 3 mg/kg, 7.5 mg/kg, 15 mg/kg, and 30 mg/kg.

Placebo Comparator: Placebo Drug: Placebo comparator
Placebo comparator




Primary Outcome Measures :
  1. Number of Participants With Treatment Emergent Treatment-Related Adverse Events (AEs) [ Time Frame: Baseline (study day -2) through study completion (study day 36 for dose cohorts <=1mg/kg, and study day 71 for dose cohorts >1mg/kg) ]
  2. Number of Participants With Clinical Laboratory Abnormalities [ Time Frame: Baseline (study day -2), study days 2, 4, 6, 8, 11, 15, 22, 29 and final study visit (study day 36 for dose cohorts <=1mg/kg, and study day 71 for dose cohorts >1mg/kg) ]
    Safety laboratory includes Hematology, Chemistry, Urinalysis, prothrombin time/international normalized ratio, partial thromboplastin time, D dimer, and fibrinogen

  3. Number of Participants With Categorical Vital Signs Data [ Time Frame: Baseline (study day 1, pre-dose), study days 1 (post dose), 2, 3, 4, 6, 8, 11, 15, 22, and end of study visit (study day 36 for dose cohorts <=1mg/kg, and study day 71 for dose cohorts >1mg/kg) ]
    Vital signs include blood pressure, pulse rate, and oral body temperature. Number of participants with maximum increase from Baseline in sitting SBP and DBP of greater than or equal to 30 mmHg will be reported

  4. Number of Participants With Abnormal Electrocardiogram (ECG) [ Time Frame: Baseline (study day 1, pre-dose), study days 1 (post dose), 2, 4, 6, 8, 11, 22, and end of study visit (study day 36 for dose cohorts <=1mg/kg, and study day 71 for dose cohorts >1mg/kg) ]
    Criteria for ECG abnormalities: maximum PR interval >=300 milliseconds (msec) and maximum increase PR interval increase from baseline (IFB): percent change (Pctchg) >=25 percent (%) for baseline value of >200 msec and Pctchg>=50% for baseline value of <=200 msec for PR interval, maximum QRS interval >=140 msec and a maximum IFB: Pctchg>=50%, maximum QTCF interval (Fridericia's Correction) of 450 msec to <480 msec, 480 msec to <500 msec or >=500 msec and a maximum change of <=30change<60 or >=60 msec from baseline.


Secondary Outcome Measures :
  1. Maximum Observed Plasma Concentration (Cmax) [ Time Frame: Baseline (study day 1, pre-dose), 0.5, 1, 3, 5, 8, 12 and 24 hours post dose for all cohorts. Study days 3, 4, 6, and 8 only for dose cohorts <=1mg/kg. Study day 3, 4, 6, 8, 15, 22, 29, 36, 50 and end of study visit day 71 for dose cohorts >1mg/kg ]
  2. Dose Normalized Maximum Observed Plasma Concentration Cmax [ Time Frame: Baseline (study day 1, pre-dose), 0.5, 1, 3, 5, 8, 12 and 24 hours post dose for all cohorts. Study days 3, 4, 6, and 8 only for dose cohorts <=1mg/kg. Study day 3, 4, 6, 8, 15, 22, 29, 36, 50 and end of study visit day 71 for dose cohorts >1mg/kg ]
  3. Time to Reach Maximum Observed Plasma Concentration (Tmax) [ Time Frame: Baseline (study day 1, pre-dose), 0.5, 1, 3, 5, 8, 12 and 24 hours post dose for all cohorts. Study days 3, 4, 6, and 8 only for dose cohorts <=1mg/kg. Study day 3, 4, 6, 8, 15, 22, 29, 36, 50 and end of study visit day 71 for dose cohorts >1mg/kg ]
  4. Area Under the Curve From Time Zero to Last Quantifiable Concentration (AUClast) [ Time Frame: Baseline (study day 1, pre-dose), 0.5, 1, 3, 5, 8, 12 and 24 hours post dose for all cohorts. Study days 3, 4, 6, and 8 only for dose cohorts <=1mg/kg. Study day 3, 4, 6, 8, 15, 22, 29, 36, 50 and end of study visit day 71 for dose cohorts >1mg/kg ]
    Area under the plasma concentration time-curve from zero to the last measured concentration (AUClast)

  5. Dose Normalized Area Under the Curve From Time Zero to Last Quantifiable Concentration (AUClast) [ Time Frame: Baseline (study day 1, pre-dose), 0.5, 1, 3, 5, 8, 12 and 24 hours post dose for all cohorts. Study days 3, 4, 6, and 8 only for dose cohorts <=1mg/kg. Study day 3, 4, 6, 8, 15, 22, 29, 36, 50 and end of study visit day 71 for dose cohorts >1mg/kg ]
  6. Area Under the Curve From Time Zero to Extrapolated Infinite Time (AUCinf) [ Time Frame: Baseline (study day 1, pre-dose), 0.5, 1, 3, 5, 8, 12, and 24 hours post dose study day 1, study days 3, 4, 6, 8, 15, 22, 29, 36, 50 and study day 71 for dose cohorts >1mg/kg) ]
    AUCinf = Area under the plasma concentration versus time curve (AUC) from time zero (pre-dose) to extrapolated infinite time (0-inf). It is obtained from AUC (0-t) plus AUC (t-inf).

  7. Dose Normalized Area Under the Curve From Time Zero to Extrapolated Infinite Time (AUCinf) [ Time Frame: Baseline (study day 1, pre-dose), 0.5, 1, 3, 5, 8, 12 and 24 hours post dose for all cohorts. Study days 3, 4, 6, and 8 only for dose cohorts <=1mg/kg. Study day 3, 4, 6, 8, 15, 22, 29, 36, 50 and end of study visit day 71 for dose cohorts >1mg/kg ]
  8. Plasma Decay Half-Life (t1/2) [ Time Frame: Baseline (study day 1, pre-dose), 0.5, 1, 3, 5, 8, 12 and 24 hours post dose for all cohorts. Study days 3, 4, 6, and 8 only for dose cohorts <=1mg/kg. Study day 3, 4, 6, 8, 15, 22, 29, 36, 50 and end of study visit day 71 for dose cohorts >1mg/kg ]
    Plasma decay half-life is the time measured for the plasma concentration to decrease by one half.

  9. Apparent Clearance (CL) [ Time Frame: Baseline (study day 1, pre-dose), 0.5, 1, 3, 5, 8, 12 and 24 hours post dose for all cohorts. Study days 3, 4, 6, and 8 only for dose cohorts <=1mg/kg. Study day 3, 4, 6, 8, 15, 22, 29, 36, 50 and end of study visit day 71 for dose cohorts >1mg/kg ]
    Steady state total body clearance equals infusion rate (zero order) divided by steady state plasma concentration of study drug (R0/Css)

  10. Incidence of Anti-Drug Antibody (ADA) [ Time Frame: Baseline, study days 15, 22, 29, and end of study visit (study day 36 for dose cohorts <=1mg/kg, and study day 71 for dose cohorts >1mg/kg) ]
  11. Characterisation of biomarker changes [ Time Frame: Baseline (study day 1, pre-dose), 1, 3, 5, 8, and 24 hours post dose, study days 3, 4, 8, 15, and end of study visit (study day 36 for dose cohorts <=1mg/kg, and study day 71 for dose cohorts >1mg/kg) ]
    Change from baseline of IL-6, TNF alpha, IFN gamma and complement C3a, Bb, and C5a



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


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Ages Eligible for Study:   18 Years to 40 Years   (Adult)
Sexes Eligible for Study:   Male
Gender Based Eligibility:   Yes
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Healthy male participants who, at the time of screening, are between the ages of 18 and 40 years, inclusive. Healthy is defined as no clinically relevant abnormalities identified by a detailed medical history, full physical examination, including oral temperature, blood pressure (BP) and pulse rate measurement, pulse oximetry, 12 lead ECG or clinical laboratory tests.
  • Evidence of a personally signed and dated informed consent document indicating that the subject has been informed of all pertinent aspects of the study.
  • Chest X ray with no evidence of current, active tuberculosis (TB) or previous inactive TB, general infections, heart failure, malignancy, or other clinically significant abnormalities taken at Screening or within 3 months prior to Screening and read by a qualified radiologist.

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 the time of dosing).
  • Participants with a history of autoimmune disorders and other conditions that compromise or impair the immune system (including but not limited to: Crohns Disease, rheumatoid arthritis, scleroderma, systemic lupus erythematosus, Graves disease, and asthma) or have a current positive result for the following; rheumatoid factor, anti-nuclear antibody, or abnormal free triiodothyronine (T3), free thyroxine (T4), thyroid stimulating hormone (TSH), or thyroid stimulating antibody (TSAb) suggestive of thyroid disease.

Subjects with a history of allergic or anaphylactic reaction to any drug including immunoglobulin

  • History of active infections within 28 days prior to the screening visit
  • Subjects with a history of or current positive results for any of the following serological tests: Hepatitis B surface antigen (HepBsAg), Hepatitis B core antibody (HepBcAb), Hepatitis C antibody (HCVAb) or human immunodeficiency virus (HIV).
  • Subjects with a history of thromboembolic events or current positive result for anti-cardiolipin antibody
  • History of TB or active, latent or inadequately treated TB infection. All positive TB test result(s) are exclusionary
  • Male subjects with partners currently pregnant; male subjects able to father children who are unwilling or unable to use a highly effective method of contraception as outlined in this protocol for the duration of the study.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03275740


Contacts
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Contact: Pfizer CT.gov Call Center 1-800-718-1021 ClinicalTrials.gov_Inquiries@pfizer.com

Locations
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Belgium
Pfizer Clinical Research Unit Recruiting
Brussels, Belgium, B-1070
Sponsors and Collaborators
Pfizer
Investigators
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Study Director: Pfizer CT.gov Call Center Pfizer

Additional Information:
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Responsible Party: Pfizer
ClinicalTrials.gov Identifier: NCT03275740     History of Changes
Other Study ID Numbers: B7801001
First Posted: September 8, 2017    Key Record Dates
Last Update Posted: March 21, 2019
Last Verified: March 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No
Plan Description: Pfizer will provide access to individual de-identified participant data and related study documents (e.g. protocol, Statistical Analysis Plan (SAP), Clinical Study Report (CSR)) upon request from qualified researchers, and subject to certain criteria, conditions, and exceptions. Further details on Pfizer's data sharing criteria and process for requesting access can be found at: https://www.pfizer.com/science/clinical_trials/trial_data_and_results/data_requests.

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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No

Additional relevant MeSH terms:
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Purpura
Purpura, Thrombocytopenic
Purpura, Thrombocytopenic, Idiopathic
Polyradiculoneuropathy
Polyradiculoneuropathy, Chronic Inflammatory Demyelinating
Blood Coagulation Disorders
Hematologic Diseases
Hemorrhage
Pathologic Processes
Skin Manifestations
Signs and Symptoms
Thrombotic Microangiopathies
Thrombocytopenia
Blood Platelet Disorders
Immune System Diseases
Hemorrhagic Disorders
Autoimmune Diseases
Autoimmune Diseases of the Nervous System
Nervous System Diseases
Demyelinating Diseases
Polyneuropathies
Peripheral Nervous System Diseases
Neuromuscular Diseases