A First in HumanTrial to Evaluate The Safety, Tolerability, And Pharmacokinetics Of PF-06755347

• ClinicalTrials.gov Identifier: NCT03275740
• Recruitment Status: Terminated
• First Posted: September 8, 2017
• Last Update Posted: February 13, 2023
• Sponsor: Pfizer
• Information provided by (Responsible Party): Pfizer

Tracking Information

• First Submitted Date: July 6, 2017
• First Posted Date: September 8, 2017
• Last Update Posted Date: February 13, 2023
• Actual Study Start Date: July 17, 2017
• Actual Primary Completion Date: January 6, 2023 (Final data collection date for primary outcome measure)

Current Primary Outcome Measures (submitted: December 17, 2021)

• Number of Participants With Treatment Emergent Treatment-Related Adverse Events (AEs) [ Time Frame: Baseline (study day -2) through study completion (study day 36 for intravenous dose cohorts 1 - 6, and study day 71 for subcutaneous dose cohorts. ]
• Number of Participants With Clinical Laboratory Abnormalities [ Time Frame: Baseline, study days 1, 2, 4, 6, 8, 11, 15, 22, 29 and 36 for i.v. dose cohorts 1 - 6, and Baseline, study days 1, 2, 3, 4, 6, 8, 11, 15, 22, 29, 36, 50 and day 71 for subcutaneous dose cohorts. ]
  Safety laboratory includes Hematology, Chemistry, Urinalysis, prothrombin time/international normalized ratio, partial thromboplastin time, D dimer, and fibrinogen
• Number of Participants With Categorical Vital Signs Data [ Time Frame: Baseline, study days 1, 2, 3, 4, 6, 8, 11, 15, 22, 29, and day 36 for i.v. dose cohorts 1 - 6 and Baseline, study days 1, 2, 3, 4, 6, 8, 11, 15, 22, 29, 36, 50 and day 71 for subcutaneous dose cohorts. ]
  Vital signs include blood pressure, pulse rate, and 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
• 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, 36 (end of study visit for intravenous dose cohorts 1 - 6, and end of study visit day 71) for subcutaneous dose cohorts. ]
  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.

Original Primary Outcome Measures (submitted: September 5, 2017)

• Number of Participants With Treatment Emergent Treatment-Related Adverse Events (AEs) [ Time Frame: Baseline (study day -1) through study completion (study day 36 for dose cohorts <=1mg/kg, and study day 71 for dose cohorts >1mg/kg) ]
• Number of Participants With Clinical Laboratory Abnormalities [ Time Frame: Baseline (study day -1), study days 2, 4, 6, 8, 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
• 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, 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
• Number of Participants With Abnormal Electrocardiogram (ECG) [ Time Frame: Baseline (study day 1, pre-dose), study days 1 (post dose), 2, 4, 6, 8, 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.

Current Secondary Outcome Measures (submitted: December 17, 2021)

• Maximum Observed Plasma Concentration (Cmax) [ Time Frame: Hours 0, 12, 24, 48, 72, 120, 168 for all cohorts. Hours 1, 3, 5, & 8 for all i.v. cohorts. Hour 36 for i.v. cohorts 1-2. Days 15, 22, 29, and 36 for subcutaneous and i.v. cohorts 5 exp & 6. Days 5, 11, 50 & 71 for subcutaneous cohorts ]
• Dose Normalized Maximum Observed Plasma Concentration Cmax [ Time Frame: Hours 0, 12, 24, 48, 72, 120, 168 for all cohorts. Hours 1, 3, 5, & 8 for all i.v. cohorts. Hour 36 for i.v. cohorts 1-2. Days 15, 22, 29, and 36 for subcutaneous and i.v. cohorts 5 exp & 6. Days 5, 11, 50 & 71 for subcutaneous cohorts ]
• Time to Reach Maximum Observed Plasma Concentration (Tmax) [ Time Frame: Hours 0, 12, 24, 48, 72, 120, 168 for all cohorts. Hours 1, 3, 5, & 8 for all i.v. cohorts. Hour 36 for i.v. cohorts 1-2. Days 15, 22, 29, and 36 for subcutaneous and i.v. cohorts 5 exp & 6. Days 5, 11, 50 & 71 for subcutaneous cohorts ]
• Area Under the Curve From Time Zero to Last Quantifiable Concentration (AUClast) [ Time Frame: Hours 0, 12, 24, 48, 72, 120, 168 for all cohorts. Hours 1, 3, 5, & 8 for all i.v. cohorts. Hour 36 for i.v. cohorts 1-2. Days 15, 22, 29, and 36 for subcutaneous and i.v. cohorts 5 exp & 6. Days 5, 11, 50 & 71 for subcutaneous cohorts ]
  Area under the plasma concentration time-curve from zero to the last measured concentration (AUClast)
• Dose Normalized Area Under the Curve From Time Zero to Last Quantifiable Concentration (AUClast) [ Time Frame: Hours 0, 12, 24, 48, 72, 120, 168 for all cohorts. Hours 1, 3, 5, & 8 for all i.v. cohorts. Hour 36 for i.v. cohorts 1-2. Days 15, 22, 29, and 36 for subcutaneous and i.v. cohorts 5 exp & 6. Days 5, 11, 50 & 71 for subcutaneous cohorts ]
• Area Under the Curve From Time Zero to Extrapolated Infinite Time (AUCinf) [ Time Frame: Hours 0, 12, 24, 48, 72, 120, 168 for all cohorts. Hours 1, 3, 5, & 8 for all i.v. cohorts. Hour 36 for i.v. cohorts 1-2. Days 15, 22, 29, and 36 for subcutaneous and i.v. cohorts 5 exp & 6. Days 5, 11, 50 & 71 for subcutaneous cohorts ]
  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).
• Dose Normalized Area Under the Curve From Time Zero to Extrapolated Infinite Time (AUCinf) [ Time Frame: Hours 0, 12, 24, 48, 72, 120, 168 for all cohorts. Hours 1, 3, 5, & 8 for all i.v. cohorts. Hour 36 for i.v. cohorts 1-2. Days 15, 22, 29, and 36 for subcutaneous and i.v. cohorts 5 exp & 6. Days 5, 11, 50 & 71 for subcutaneous cohorts ]
• Plasma Decay Half-Life (t1/2) [ Time Frame: Hours 0, 12, 24, 48, 72, 120, 168 for all cohorts. Hours 1, 3, 5, & 8 for all i.v. cohorts. Hour 36 for i.v. cohorts 1-2. Days 15, 22, 29, and 36 for subcutaneous and i.v. cohorts 5 exp & 6. Days 5, 11, 50 & 71 for subcutaneous cohorts ]
  Plasma decay half-life is the time measured for the plasma concentration to decrease by one half.
• Apparent Clearance (CL) [ Time Frame: Hours 0, 12, 24, 48, 72, 120, 168 for all cohorts. Hours 1, 3, 5, & 8 for all i.v. cohorts. Hour 36 for i.v. cohorts 1-2. Days 15, 22, 29, and 36 for subcutaneous and i.v. cohorts 5 exp & 6. Days 5, 11, 50 & 71 for subcutaneous cohorts ]
  Steady state total body clearance equals infusion rate (zero order) divided by steady state plasma concentration of study drug (R0/Css)
• Incidence of Anti-Drug Antibody (ADA) [ Time Frame: Baseline, study days 8, 15, and 36 for all dose cohorts plus day 71 for subcu cohorts ]
• Characterization of biomarker changes [ Time Frame: Day -1, hours 0, 5, 12, 24, 48, 72 for all cohorts. Hours 1 (or end of infusion, 8, 120 and days 11 & 29 for i.v. cohorts Days 5, 8, 15, 36 & 71 for subcutaneous cohorts. ]

Original Secondary Outcome Measures (submitted: September 5, 2017)

• 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 study day 1, study days 3, 4, 6, 8, 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) ]
• 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 study day 1, study days 3, 4, 6, 8, 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) ]
• 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 study day 1, study days 3, 4, 6, 8, 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) ]
• 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 study day 1, study days 3, 4, 6, 8, 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) ]
  Area under the plasma concentration time-curve from zero to the last measured concentration (AUClast)
• 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 study day 1, study days 3, 4, 6, 8, 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) ]
• 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, and end of study visit (study day 36 for dose cohorts <=1mg/kg, 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).
• 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 study day 1, study days 3, 4, 6, 8, 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) ]
• 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 study day 1, study days 3, 4, 6, 8, 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) ]
  Plasma decay half-life is the time measured for the plasma concentration to decrease by one half.
• Apparent Clearance (CL) [ 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, and end of study visit ]
  Steady state total body clearance equals infusion rate (zero order) divided by steady state plasma concentration of study drug (R0/Css)
• 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) ]

• Current Other Pre-specified Outcome Measures: Not Provided
• Original Other Pre-specified Outcome Measures: Not Provided

Descriptive Information

• Brief Title: A First in HumanTrial to Evaluate The Safety, Tolerability, And Pharmacokinetics Of PF-06755347
• 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 AND SUBCUTANEOUS DOSING IN HEALTHY ADULT MALE PARTICIPANTS AND OPEN-LABEL AFTER SINGLE SUBCUTANEOUS DOSING IN MALE AND FEMALE PARTICIPANTS WITH PERSISTENT OR CHRONIC PRIMARY IMMUNE THROMBOCYTOPENIA
• 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 males as well as adult males and females with Immune Thrombocytopenia (ITP). Pharmacokinetics and pharmacodynamics will also be evaluated.
• Detailed Description: Not Provided
• Study Type: Interventional
• Study Phase: Phase 1

Study Design

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 in healthy male participants. Masking will not be applied for participants with ITP (all ITP participants will receive PF-06755347).

Primary Purpose: Treatment

Condition

• Healthy
• Primary Immune Thrombocytopenia
• Polyradiculoneuropathy, Chronic Inflammatory Demyelinating

Intervention

• Drug: PF-06755347 intravenous healthy participant
  Single doses of PF-06755347 will be administered intravenously dose levels 1, 2, 3, 4, 5, and 6.
• Drug: Placebo intravenous healthy participant
  Placebo comparator
• Drug: PF-06755347 subcutaneous healthy participant
  single doses of PF-06755347 will be administered subcutaneously at dose levels of SC1, SC2, SC3, SC4, and SC5.
• Drug: Placebo subcutaneous healthy participant
  placebo comparator
• Drug: PF-06755347 subcutaneous ITP
  single doses of PF-06755347 will be administered subcutaneously at 2 dose levels tested in healthy participants

Study Arms

• Experimental: PF-06755347 intravenous healthy participant
  intravenous administration
  Intervention: Drug: PF-06755347 intravenous healthy participant
• Placebo Comparator: Placebo intravenous healthy participant
  intravenous administration
  Intervention: Drug: Placebo intravenous healthy participant
• Experimental: PF-06755347 subcutaneous healthy participant
  subcutaneous administration
  Intervention: Drug: PF-06755347 subcutaneous healthy participant
• Placebo Comparator: Placebo subcutaneous healthy participant
  subcutaneous administration
  Intervention: Drug: Placebo subcutaneous healthy participant
• Experimental: PF-06755347 subcutaneous ITP
  subcutaneous
  Intervention: Drug: PF-06755347 subcutaneous ITP

• Publications *: Not Provided

Recruitment Information

• Recruitment Status: Terminated
• Actual Enrollment (submitted: February 9, 2023): 58
• Original Estimated Enrollment (submitted: September 5, 2017): 73
• Actual Study Completion Date: January 6, 2023
• Actual Primary Completion Date: January 6, 2023 (Final data collection date for primary outcome measure)

Eligibility Criteria

Inclusion Criteria Healthy male participants:

• at the time of screening, are between the ages of 18 and 55 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 for Healthy male participants:

• 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.
• 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.
• Inclusion Criteria for ITP participants:

Female participants may be of childbearing potential or non-childbearing potential.

-Diagnosis of Primary ITP. ITP must be diagnosed in accordance with established guidelines. ITP duration-Persistent (>3 months and ≤12 months) OR Chronic (>12 months).

AND

• Platelet count 30-75 x 10E9/L (inclusive) with criteria achieved on 2 qualifying counts at least 5 days apart and within approx. 10 days of dosing

• Participants must have received and responded to IVIg or corticosteroids as treatment for ITP (response is defined as achievement of platelet count >50 x 109/L and doubling of platelet count from baseline).

  --Evidence of a personally signed and dated informed consent document indicating that the subject has been informed of all pertinent aspects of the study.

• BMI of 17.5 to 30.5 kg/m2 and a total body weight >40 kg (88 lbs).

Exclusion Criteria for ITP participants

• History of clinically significant hematological (other than ITP), renal, endocrine, metabolic, pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric, neurologic, or allergic disease (but excluding untreated, asymptomatic, seasonal allergies at the time of dosing).
• Chest X-ray with evidence of current, active TB, previous inactive TB, general infections, heart failure, malignancy, or other clinically significant abnormalities.

Chest x-ray must be taken at Screening or within 3 months prior to Screening and read by a qualified radiologist.

• Any bleeding event requiring medical evaluation or treatment in the 4 weeks prior to screening or current bleeding event that requires treatment.
• Scheduled or anticipated invasive procedures (eg, surgery, dental procedures) within 28 days following PF-06755347 dosing.
• Splenectomy within ≤180 days prior to PF-06755347 dosing or splenectomy planned during the period of the study.
• History of any active autoimmune disorder (other than ITP) or other conditions that may compromise or impair the immune system (including but not limited to: Crohn's Disease, rheumatoid arthritis, scleroderma, systemic lupus erythematosus, Graves' disease, and asthma).
• History of allergic or anaphylactic reaction to any drug including immunoglobulin.
• History of active infections within 28 days prior to the screening visit.
• History of Hepatitis B, Hepatitis C or HIV or current positive results for any of the following serological tests - HBsAg, HBcAb, HCVAb or HIV.
• History of thromboembolic events
• Hemoglobin <9 g/dL.
• Positive Direct Coombs test

Sex/Gender

• Sexes Eligible for Study: All

• Ages: 18 Years to 55 Years (Adult)
• Accepts Healthy Volunteers: Yes
• Contacts: Contact information is only displayed when the study is recruiting subjects
• Listed Location Countries: Belgium, New Zealand, Spain, United Kingdom, United States

Administrative Information

• NCT Number: NCT03275740
• Other Study ID Numbers: B7801001; 2018-003315-21 ( EudraCT Number )
• Has Data Monitoring Committee: No

U.S. FDA-regulated Product

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

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.

• Current Responsible Party: Pfizer
• Original Responsible Party: Same as current
• Current Study Sponsor: Pfizer
• Original Study Sponsor: Same as current
• Collaborators: Not Provided

Investigators

• Study Director: Pfizer CT.gov Call Center; Pfizer

• PRS Account: Pfizer
• Verification Date: February 2023