Study to Assess the Safety, Tolerability, PK, ECG Effects, Food Effect, and Drug-drug Interaction (DDI) of Hormonal Contraceptives of PTI-428 in Healthy Female Volunteers

NCT ID: NCT02846142

Last Updated: 2018-05-24

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 94 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2016-06-30
• Study Completion Date: 2017-03-31

Brief Summary

This trial will consist of three parts: the first two parts will enroll healthy female volunteers into a single ascending dose (SAD) and multiple ascending dose (MAD) treatment groups.

The SAD treatment group is comprised of at least 3 cohorts where subjects will be randomized to a single dose of either PTI-428 or placebo and will be followed for 7 days post dose. A total of 24 subjects are anticipated to participate in this part of the study.

Following the conclusion of the respective SAD level dose groups and after sufficient review of study data and approval by the SRC, a second set of healthy adult female subjects will participate in an assigned MAD treatment group. The MAD treatment group is comprised of 3 cohorts where subjects will be randomized to either PTI-428 or placebo and will be followed for a total of 14 days. The SRC will convene after the completion of each cohort to evaluate safety, PK and other relevant data. The SRC will determine whether to proceed to the next planned dose level, to reduce the dose, or to stop the study. The next cohort may commence only after written SRC approval. A total of 24 subjects are anticipated to participate in this part of the study.

Following completion of the SAD and MAD, 40 female healthy volunteers will participate in two treatment periods of the DDI study component: Treatment period A will consist of once daily oral contraceptive (OC) for 28-days (21-day hormonal active + 7 days off).

Treatment period B will randomize subjects to PTI-428 or placebo in combination with once daily OC for 28 days (21-day hormonal active and PTI-428 or placebo + 7 days off). Following completion of the subjects' second treatment period, they will be followed for 7-days after their last dose.

Conditions

Healthy Volunteer

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

SAD PTI-428

The safety, tolerability, and pharmacokinetic profile of PTI-428 will be evaluated following a single dose of PTI-428. Three cohorts are planned for evaluation where subjects will be randomized to PTI-428 or placebo.The subjects will be followed for 7 days post dose.

Group Type: ACTIVE_COMPARATOR

PTI-428

Intervention Type: DRUG

SAD placebo

The safety, tolerability, and pharmacokinetic profile of PTI-428 will be evaluated following a single dose of PTI-428. Three cohorts are planned for evaluation where subjects will be randomized to PTI-428 or placebo.The subjects will be followed for 7 days post dose.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: OTHER

MAD PTI-428

Following the conclusion of the respective SAD level dose groups and after sufficient review of study data and approval by the SRC, a second set of healthy adult female subjects will participate in an assigned MAD treatment group. The MAD treatment group is comprised of 3 cohorts. Subjects will be randomized to either PTI-428 or placebo. Each dose will be administered once daily (QD) for a total of 7 days. Follow up visits will occur on Days 12 and 14.

Group Type: ACTIVE_COMPARATOR

PTI-428

Intervention Type: DRUG

MAD placebo

Following the conclusion of the respective SAD level dose groups and after sufficient review of study data and approval by the SRC, a second set of healthy adult female subjects will participate in an assigned MAD treatment group. The MAD treatment group is comprised of 3 cohorts. Subjects will be randomized to either PTI-428 or placebo. Each dose will be administered once daily (QD) for a total of 7 days. Follow up visits will occur on Days 12 and 14.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: OTHER

OC (ethinyl estradiol and levonorgestrel) DDI Period A

Treatment period A will consist of once daily oral contraceptive (OC) for 28-days (21-day hormonal active + 7 days off).

Group Type: EXPERIMENTAL

ethinyl estradiol and levonorgestrel

Intervention Type: DRUG

OC (ethinyl estradiol and levonorgestrel) DDI Period B

Treatment period B will randomize subjects to PTI-428 or placebo in combination with once daily OC daily for 28 days (21-day hormonal active + 7 days off).

Group Type: ACTIVE_COMPARATOR

PTI-428

Intervention Type: DRUG

ethinyl estradiol and levonorgestrel

Intervention Type: DRUG

OC (ethinyl estradiol and levonorgestrel) DDI

Treatment period B will randomize subjects 4:1 to PTI-428 or placebo in combination with once daily OC daily for 28 days (21-day hormonal active + 7 days off).

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: OTHER

ethinyl estradiol and levonorgestrel

Intervention Type: DRUG

Interventions

PTI-428

Intervention Type: DRUG

Placebo

Intervention Type: OTHER

ethinyl estradiol and levonorgestrel

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Adult females age 18 - 55 years old, inclusive, at the time of informed consent.
• For the DDI Oral Contraceptive Cohort, women of child bearing potential with intact ovarian function by medical history and history of regular menstrual. cycles.
• Body mass index (BMI) ≥18 < 30 kg/m2.
• Subject must be non-smoker and non-tobacco user for a minimum of 30 days prior to screening and for the duration of the study.
• Subject understands the full nature and purpose of the study, including possible risks and side effects, and is willing and able to comply with all compulsory study procedures and provides informed consent/permission prior to any study procedures being performed.

Exclusion Criteria

• History or current evidence of any clinically significant cardiac, endocrinologic, hematologic, hepatobiliary, immunologic, metabolic, urologic, pulmonary, neurologic, dermatologic, psychiatric, renal, or other major disease, as determined by the Investigator.
• Abnormal liver function as defined by:
• Aspartate aminotransferase (AST), alanine aminotransferase (ALT) or bilirubin > 1.5 x upper limit of the normal range.
• Abnormal renal function at screening defined as:
• Creatinine clearance < 80mL/min using the Cockroft-Gault equation.
• No clinically significant screening results that would exclude subject from the study (e.g., medical histories, physical examination, ECGs, vital signs,and laboratory profiles) as deemed by the investigator.
• Platelet count < 150,000 cell/mm3
• Participation in another clinical trial or treatment with an investigational agent within 30 days or 5 half-lives, whichever is longer, prior to Study Day 1.
• History of cancer within the past five years (excluding non-melanoma skin cancer).
• History of alcohol or drug abuse or dependence within 12 months of screening as determined by the Investigator.
• Positive urine screen for prohibited drugs (cocaine, cannabinoids, nicotine [urine cotinine is the detection mechanism for nicotine], opiates, barbiturates, amphetamines, and benzodiazepines) or positive alcohol test at screening.
• Positive blood screen for human immunodeficiency virus (HIV), hepatitis B surface antigen (HBsAg), or hepatitis C virus antibody (HCVAb).
• Clinically significant infection within 3 months of screening as determined by the Investigator.
• Known or suspected hypersensitivity or idiosyncratic reaction to study medication or any components thereof.
• Has donated blood within 3 months of screening or plans to donate blood within 3 months of study completion.
• Pregnant or nursing women.
• Any conditions that, in the opinion of the Investigator, would make the subject unsuitable for enrollment or could interfere with the subject's participation in or completion of the study.
• Females of child-bearing potential, unless they are willing to use highly effective methods of contraception during participation in the clinical study and for 30 days after termination from study.
• Use of prohibited medications within 14 days prior to dosing of study drug.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 55 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: Yes

Sponsors

Proteostasis Therapeutics, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Overland Park, Kansas, United States

Countries

United States

Other Identifiers

PTI-428-02

Identifier Type: -

Identifier Source: org_study_id