Relative Bioavailability Study and Food Effect Study of TT-00420 (Tinengotinib) Capsule and Tablet Formulations in Healthy Volunteers

Healthy Clinical Trial

Official title:

A Phase I, Single-Center, Open-Label, 3-Way Crossover, Randomized Single Dose Study to Evaluate the Food Effect on the Pharmacokinetics of TT-00420 Tablet and to Determine the Relative Bioavailability of TT-00420 Tablet Versus TT-00420 Capsule in Adult Healthy Volunteers

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04705922
• Other study ID #: TT420HV1102
• Status: Completed
• Phase: Phase 1
• Start date: December 29, 2020
• Est. completion date: July 23, 2021

Study information

• Verified date: December 2023
• Source: TransThera Sciences (Nanjing), Inc.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study is an open-label, 3-way crossover randomized study in adult healthy volunteers to evaluate the relative bioavailability of TT-00420 tablet and capsule formulations and to evaluate food effect on the pharmacokinetics of TT-00420 tablet.

Description:

Subjects will be randomized to one of three treatment sequences. Each sequence will contain up to 8 subjects. In each treatment sequence, subjects undergo a baseline/screening period, three treatment periods, and a follow-up visit. Subjects will be administered a single dose of TT-00420 on Day 1 of either TT-00420 tablet under fed condition, TT-00420 tablet under fasting condition, or capsule under fasting condition and crossed over after at least a 14-day washout period.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 24
• Est. completion date: July 23, 2021
• Est. primary completion date: March 7, 2021
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 64 Years

Eligibility

Inclusion Criteria:

1. Male or female subjects between 18 and 64 years of age inclusive, at the time of signing the informed consent.

2. Body mass index (BMI) between 18 and 32 kg/m2, inclusive, and weighs at least 50 kg.

3. Healthy as determined by the investigator based on medical history, clinical laboratory results (serum chemistry, hematology, urinalysis, and serology), vital sign measurements, 12-lead electrocardiogram (ECG) results, and physical examination findings. A subject with a clinical abnormality or laboratory parameters outside the reference range for the population being studied may be included only, if per the investigator discretion, the investigator judges and documents that the finding is unlikely to introduce additional risk factors and will not interfere with the study procedures.

4. Male subjects must not donate sperm starting at Screening, throughout the study period and for at least 90 days after final study drug administration.

5. Male subjects with female sexual partner(s) of reproductive potential may be enrolled

if the male:

1. is documented to be surgically sterile (i.e., successfully vasectomized), or

2. agrees to use 2 methods of highly effective contraception and agree to refrain from sperm donation from the time of Screening through 90 days post-doseHighly effective includes male condom with spermicide PLUS an effective contraceptive for the female partner that includes: OCPs, long-acting implantable hormones, injectable hormones, a vaginal ring or IUD

6. If female, is of non-childbearing potential, meeting the following requirements:

1. pre-menopausal with documentation of surgical sterilization (i.e., hysterectomy, bilateral tubal ligation, bilateral oophorectomy, or bilateral salpingectomy at least 3 months prior to study entry), or

2. post-menopausal defined as amenorrhea for at least 12 months following cessation of all exogenous hormonal treatments and with follicle-stimulating hormone (FSH) level = 40 mIU/mL at Screening

7. Able to sign the informed consent and comply with the protocol.

Exclusion Criteria:

1. Any history of clinically serious disease.

2. Any active or unstable clinically significant medical condition as judged by the Investigator.

3. History or presence of gastrointestinal, hepatic or renal disease, or any other condition known to interfere with absorption, distribution, metabolism, or excretion of drugs

4. Hypersensitivity or allergy to any of the study drugs or drugs of similar chemical classes.

5. Hypersensitivity or allergy for components of the prescribed meal

6. Received any investigational drug within 30 days or 5 half-lives(whichever is longer, if known) before the study.

7. Subject who has undergone major surgery = 2 months before study drug administration.

8. Impaired cardiac function including clinically significant arrhythmias or clinically significant abnormality in clinical test, including but not limited to any of the following at Screening and Admission, repeat testing is allowed for verification, at

the discretion of the Investigator:

1. Heart rate < 45 beats per minute (bpm) or > 90 bpm.

2. Systolic blood pressure (SBP) < 90 mmHg or > 140 mmHg; diastolic blood pressure (DBP) < 50 mmHg or > 90 mmHg.

3. Average of the 3 QT intervals corrected using Fridericia's formula (QTcF) > 450 milliseconds.

4. Troponin I at screening > upper limit of normal (ULN).

5. Second degree or higher Atrioventricular block on ECG.

9. Subject who has a known history of, or a positive test result for, hepatitis B surface antigen (HBsAg), immunoglobulin M (IgM) antibody to hepatitis B core antibody (anti-HBc) (IgM anti-HBc), hepatitis C virus antibody (anti-HCV), or human immunodeficiency virus (HIV) types 1 or 2, or syphilis at Screening.

10. Subject with a history of severe visual diseases; or visual changes including flushing lights, blurry vision, color changes, or other visual changes.

11. Subject who has used prescription or over-the-counter (OTC) medication (other than = 2 g/day paracetamol [acetaminophen] or = 800-mg/day ibuprofen), vitamins, or herbal remedies, within 2 weeks or 5 half-lives (if known) before study drug administration, whichever is longer.

12. Subject who has had a loss of more than 100 mL blood (e.g., a blood donation) within 2 months before study drug administration, or has received any blood, plasma, or platelet transfusions within 3 months before Admission, or plans to donate blood during the study or within 3 months after the study.

13. Subject who has a history of alcohol abuse (defined as an alcohol intake more than 21 units for males and 14 units for females per week) or a history of drug abuse within the 6 months before study drug administration, or a history of substance abuse deemed significant by the Investigator.

14. Subject who smokes cigarettes or uses other nicotine-containing products (e.g., snuff, nicotine patch, nicotine chewing gum, mock cigarettes, or inhalers), and has done so in the 3 months prior to Screening.

15. Subject who has a positive test for alcohol or drugs of abuse (opiates, methadone, buprenorphine, methamphetamine, cocaine, cannabinoids, amphetamines, or cotinine) at Screening or Admission.

16. Subject is unable to complete this study for other reasons or the Investigator believes that he or she should be excluded.

Related Conditions & MeSH terms

• Healthy

Intervention

Drug:
• TT-00420 Capsule
TT-00420 capsule formulation, administered orally
• TT-00420 Tablet
TT-00420 tablet formulation, administered orally

Locations

Country	Name	City	State
United States	Pharmaron CPC	Baltimore	Maryland

Sponsors (1)

Lead Sponsor	Collaborator
TransThera Sciences (Nanjing), Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Area under the curve (AUC0-8) of TT-00420	Blood samples will be collected at indicated time points for pharmacokinetic analysis of TT-00420.	From pre-dose up to 240 hours post-dose each period (each period is 14 days)
Primary	Area under the curve (AUC0-t) of TT-00420	Blood samples will be collected at indicated time points for pharmacokinetic analysis of TT-00420.	From pre-dose up to 240 hours post-dose each period (each period is 14 days)
Primary	Maximum observed concentration (Cmax) of TT-00420	Blood samples will be collected at indicated time points for pharmacokinetic analysis of TT-00420.	From pre-dose up to 240 hours post-dose each period (each period is 14 days)
Secondary	Number of participants with adverse events (AEs)		From admission up to 10 days following discharge
Secondary	Incidence of abnormal physical examinations		At baseline and from admission to discharge, up to 12 days per period (each period is 14 days)
Secondary	Incidence of abnormal clinical laboratory tests		At baseline and from admission to discharge, up to 12 days per period (each period is 14 days)
Secondary	Incidence of abnormal vital signs		At baseline and from admission to discharge, up to 12 days per period (each period is 14 days)
Secondary	Incidence of abnormal weight		At baseline and from admission to discharge, up to 12 days per period (each period is 14 days)
Secondary	Incidence of abnormal 12-lead electrocardiogram		At baseline and from admission to discharge, up to 12 days per period (each period is 14 days)
Secondary	Half life (t1/2) of TT-00420	Blood samples will be collected at indicated time points for pharmacokinetic analysis of TT-00420.	From pre-dose up to 240 hours post-dose each period (each period is 14 days)
Secondary	Time of maximum concentration (tmax) of TT-00420	Blood samples will be collected at indicated time points for pharmacokinetic analysis of TT-00420.	From pre-dose up to 240 hours post-dose each period (each period is 14 days)
Secondary	Volume of distribution (Vd/F) of TT-00420	Blood samples will be collected at indicated time points for pharmacokinetic analysis of TT-00420.	From pre-dose up to 240 hours post-dose each period (each period is 14 days)
Secondary	Clearance (CL/F) of TT-00420	Blood samples will be collected at indicated time points for pharmacokinetic analysis of TT-00420.	From pre-dose up to 240 hours post-dose each period (each period is 14 days)