Single Dose Bioavailability and Ethnobridging PK Study in Healthy Subjects

Overview

This is a Phase 1, 2-part, open-label study. Part A will be a formulation bridging and food effect study in healthy adult subjects. Part B will be an assessment of pharmacokinetics (PK) in healthy adult Chinese subjects.

Full Title of Study: “A Phase 1, Two-Part, Open-Label Study to Assess the Relative Bioavailability of Two TD-1473 Tablet Formulations Under Fasted and Fed Conditions in Healthy Subjects and the Pharmacokinetics of TD-1473 in Healthy Chinese Subjects”

Study Type

  • Study Type: Interventional
  • Study Design
    • Allocation: Randomized
    • Intervention Model: Crossover Assignment
    • Primary Purpose: Treatment
    • Masking: None (Open Label)
  • Study Primary Completion Date: April 2021

Detailed Description

In study Part A, healthy adult subjects will receive the following treatments in a cross-over design with a ≥10-day washout period between doses:

- Treatment A: Single dose of [Tablet A] TD-1473 proposed commercial tablet formulation on Day 1 in a fasted state;

- Treatment B: Single dose of [Tablet A] TD-1473 proposed commercial tablet formulation on Day 1 in a fed state;

- Treatment C: Single dose of [Tablet B] TD-1473 current clinical tablet formulation on Day 1 in a fasted state;

- Treatment D: Single dose of [Tablet B] TD-1473 current clinical tablet formulation on Day 1 in a fed state.

In study Part B, healthy adult Chinese subjects will receive Treatment A: Single dose of [Tablet A] TD-1473 proposed commercial tablet formulation on Day 1 in a fasted state.

Interventions

  • Drug: TD-1473 [Tablet A]
    • TD-1473 [Tablet A] (1 Tablet = Dose A) proposed commercial tablet formulation
  • Drug: TD-1473 [Tablet B]
    • TD-1473 [Tablet B] (2 Tablets = Dose A) current clinical tablet formulation

Arms, Groups and Cohorts

  • Experimental: Part A, Sequence 1
    • Part A, Sequence 1 = Treatment (Tx) C, Tx A, Tx C, Tx A Single oral dose of treatment on Day 1 of each period in a 4-way crossover design with a ≥10-day washout between treatments
  • Experimental: Part A, Sequence 2
    • Part A, Sequence 2: Tx D, Tx B, Tx D, Tx B Single oral dose of treatment on Day 1 of each period in a 4-way crossover design with a ≥10-day washout period between treatments
  • Experimental: Part A, Sequence 3
    • Part A, Sequence 3: Tx C, Tx A, Tx D, Tx B Single oral dose of treatment on Day 1 of each period in a 4-way crossover design with a ≥10-day washout period between treatments
  • Experimental: Part A, Sequence 4
    • Part A, Sequence 4: Tx D, Tx B, Tx C, Tx A Single oral dose of treatment on Day 1 of each period in a 4-way crossover design with a ≥10-day washout period between treatments
  • Experimental: Part A, Sequence 5
    • Part A, Sequence 5: Tx A, Tx C, Tx A, Tx C Single oral dose of treatment on Day 1 of each period in a 4-way crossover design with a ≥10-day washout period between treatments
  • Experimental: Part A, Sequence 6
    • Part A, Sequence 6: Tx B, Tx D, Tx B, Tx D Single oral dose of treatment on Day 1 of each period in a 4-way crossover design with a ≥10-day washout period between treatments
  • Experimental: Part A, Sequence 7
    • Part A, Sequence 7: Tx A, Tx C, Tx B, Tx D Single oral dose of treatment on Day 1 of each period in a 4-way crossover design with a ≥10-day washout period between treatments
  • Experimental: Part A, Sequence 8
    • Part A, Sequence 8: Tx B, Tx D, Tx A, Tx C Single oral dose of treatment on Day 1 of each period in a 4-way crossover design with a ≥10-day washout period between treatments
  • Experimental: Part B,Treatment A
    • Single oral dose of Treatment A on Day 1

Clinical Trial Outcome Measures

Primary Measures

  • AUC0-t
    • Time Frame: Predose and at prespecified time points up to 5 days after dosing on Day 1 of each period
    • Area under the concentration-time curve, from time 0 to the last observed non-zero concentration (AUC0-t) of TD-1473 in Plasma
  • AUC0-inf
    • Time Frame: Predose and at prespecified time points up to 5 days after dosing on Day 1 of each period
    • Area under the concentration-time curve, from time 0 extrapolated to infinity (AUC0-inf) of TD-1473 in Plasma
  • Cmax
    • Time Frame: Predose and at prespecified time points up to 5 days after dosing on Day 1 of each period
    • Maximum observed concentration (Cmax) of TD-1473 in Plasma

Secondary Measures

  • Adverse events
    • Time Frame: Day 1 through Day 7 of each period
    • Number and severity of treatment emergent adverse events.

Participating in This Clinical Trial

Inclusion Criteria

  • Subject is a non-smoking male or female adult
  • Subject (females) must be of non-childbearing potential or if of childbearing potential, subject must not be pregnant or breastfeeding, and must agree to use highly effective birth control and must not donate ova through 30 days after last dose of study drug.
  • Subject (males) must agree to use contraception to prevent pregnancy/partner exposure and must not donate sperm through 30 days after last dose of study drug.
  • Subject has a body mass index (BMI) 19 to 30 kg/m^2, inclusive and weighs at least 50 kg
  • Subject is healthy as determined by the Principal Investigator or designee based on medical history and physical examinations performed at Screening and Day -1 of Period 1
  • Subject must be willing and able to comply with the study diet, willing to abstain from strenuous physical activity which could cause muscle aches or injury, including contact sports for a period of 48 hours prior to study and through follow-up visit.
  • Subject must be willing and able to give and understand written informed consent, communicate well with the PI, and comply with the study procedures, requirements and restrictions
  • Part B: subject was born in China, with 2 Chinese biological parents and 4 Chinese grandparents as confirmed by interview, has lived no longer than 10 years outside of China, and has had no significant change in lifestyle, including diet, since leaving China

Exclusion Criteria

  • Subject is planning to conceive a child during the study or within 1 month after the last dose of TD 1473
  • Subject has evidence or history of clinically significant allergic disease, hematological, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric, or neurological disease
  • Subject has history of venous thrombosis
  • Subject has any clinically significant abnormalities in the results of laboratory evaluations, or liver function tests exceeding the upper limit of normal in the screening or pre-dose period
  • Subject has creatinine clearance as calculated by Cockcroft-Gault formula <90mL/min at screening or pre-dose period.
  • Subject has any medical condition possibly affecting drug absorption
  • Subject has history of lymphoma, leukemia, or other types of malignancy
  • Subject previously participated in a study for TD 1473 and/or subject has previously taken tofacitinib or other JAK inhibitors.
  • Subject participated in another clinical trial of an investigational drug (or medical device) within 30 days
  • Subject is unwilling to abstain from ingestion of caffeine or xanthine-containing products
  • Subject is unwilling to abstain from alcohol beginning 24 hours prior to study start
  • Subject has history of alcoholism or drug abuse
  • Female subject who is pregnant and/or lactating
  • Subject has positive results at Screening for human immunodeficiency virus (HIV), hepatitis A virus (HAV) antibodies, hepatitis B virus antigen (HBsAg), hepatitis B core antibodies (HBcAb), or hepatitis C virus (HCV) antibody
  • Subject has confirmed or suspected severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection (COVID-19)
  • Subject consumed grapefruit/Seville orange and/or grapefruit juice within 14 days prior to study
  • Subject consumed cruciferous vegetables (e.g., kale, broccoli, watercress, collard greens, kohlrabi, Brussels sprouts, mustard greens) or charbroiled meats beginning 7 days prior to study start and is unwilling to abstain from consuming such vegetables during the study
  • Subject uses or has used nicotine-containing products within 6 months prior to study start
  • Subject has acute illness (GI illness, infection (e.g., influenza) or know inflammatory process) at screening or pre-dose period.
  • Subject has poor venous access that limits phlebotomy
  • Subject donated blood or had significant blood loss within 56 days prior to study start
  • Subject donated plasma within 7 days prior to study start
  • Subject has abnormal screening ECG based on certain parameters or designated by the PI or designee to be clinically significant.
  • Subject has personal or known family history of congenital long QT syndrome or known family history of sudden death
  • Subject has history of hypersensitivity to drugs with a clinically significant reaction or any clinically significant hypersensitivities
  • Subject has known hypersensitivity to contents of the study drug including excipients, or drugs from a similar chemical class as TD-1473
  • Subject has history of severe allergic reaction or severe hypersensitivity or idiosyncratic reaction to any food, medication, insect or bee sting, or previous status asthmaticus (e.g., acute severe asthma attacks)
  • Subject has history of latent or active tuberculosis
  • Subject received a live viral vaccine within 8 weeks of study start
  • Subject, who, for any reason, is deemed by the Principal Investigator, designee, or Sponsor to be inappropriate for this study or have any condition which would confound or interfere with the evaluation of the safety, tolerability, and PK of the investigational drug or prevent compliance with the study protocol

Gender Eligibility: All

Minimum Age: 19 Years

Maximum Age: 55 Years

Are Healthy Volunteers Accepted: Accepts Healthy Volunteers

Investigator Details

  • Lead Sponsor
    • Theravance Biopharma
  • Provider of Information About this Clinical Study
    • Sponsor
  • Overall Official(s)
    • Study Director, Study Director, Theravance Biopharma
  • Overall Contact(s)
    • Theravance Biopharma Call Center, 1-855-633-8479, medinfo@theravance.com

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