A Study to Investigate the Safety, Tolerability, and Pharmacokinetics of KYN-5356 in Healthy Subjects Aged 18 to 55 Years

NCT ID: NCT06225115

Last Updated: 2024-12-04

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 72 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-12-21
• Study Completion Date: 2024-10-07

Brief Summary

This first-in-human clinical trial with a randomized, double-blind, placebo-controlled, dose-escalation study design is regarded as standard to test the safety, tolerability, and pharmacokinetics of KYN-5356.

The study comprises 3 parts:

Part 1: Single Ascending Dose study Part 2: Multiple Ascending Dose study Part 3: Food Effect study

The aim of Parts 1 and 2 of the study is to evaluate the safety and tolerability following single and multiple ascending doses of KYN-5356.

The secondary aim is to evaluate the pharmacokinetics (PK) of escalating single and multiple doses of KYN-5356. In Part 2, cerebrospinal fluid will be sampled to explore PK and pharmacodynamic effects of KYN-5356.

The potential effect of food intake on the disposition of KYN-5356 following a single oral dose will be evaluated in Part 3. Part 3 is an open-label, randomized, 2 period, 2 sequence design.

Conditions

Cognitive Dysfunction; Schizophrenia

Study Design

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

Study Groups

SAD Cohort 1

Single-Ascending Dose Cohort 1. Intervention: KYN-5356 A mg or placebo, single dose, oral tablet

Group Type: EXPERIMENTAL

KYN-5356

Intervention Type: DRUG

KYN-5356, oral tablet

placebo

Intervention Type: DRUG

placebo, oral tablet

SAD Cohort 2

Single-Ascending Dose Cohort 2. Intervention: KYN-5356 B mg or placebo, single dose, oral tablet

Group Type: EXPERIMENTAL

KYN-5356

Intervention Type: DRUG

KYN-5356, oral tablet

placebo

Intervention Type: DRUG

placebo, oral tablet

SAD Cohort 3

Single-Ascending Dose Cohort 3. Intervention: KYN-5356 C mg or placebo, single dose, oral tablet

Group Type: EXPERIMENTAL

KYN-5356

Intervention Type: DRUG

KYN-5356, oral tablet

placebo

Intervention Type: DRUG

placebo, oral tablet

SAD Cohort 4

Single-Ascending Dose Cohort 4. Intervention: KYN-5356 D mg or placebo, single dose, oral tablet

Group Type: EXPERIMENTAL

KYN-5356

Intervention Type: DRUG

KYN-5356, oral tablet

placebo

Intervention Type: DRUG

placebo, oral tablet

SAD Cohort 5

Single-Ascending Dose Cohort 5. Intervention: KYN-5356 E mg or placebo, single dose, oral tablet

Group Type: EXPERIMENTAL

KYN-5356

Intervention Type: DRUG

KYN-5356, oral tablet

placebo

Intervention Type: DRUG

placebo, oral tablet

MAD Cohort 1

Multiple-Ascending Dose Cohort 1. Intervention: KYN-5356 G mg or placebo, oral tablets for 7 days

Group Type: EXPERIMENTAL

KYN-5356

Intervention Type: DRUG

KYN-5356, oral tablet

placebo

Intervention Type: DRUG

placebo, oral tablet

MAD Cohort 2

Multiple-Ascending Dose Cohort 2. Intervention: KYN-5356 H mg or placebo, oral tablets for 7 days

Group Type: EXPERIMENTAL

KYN-5356

Intervention Type: DRUG

KYN-5356, oral tablet

placebo

Intervention Type: DRUG

placebo, oral tablet

MAD Cohort 3

Multiple-Ascending Dose Cohort 3. Intervention: KYN-5356 I mg or placebo, oral tablets for 7 days

Group Type: EXPERIMENTAL

KYN-5356

Intervention Type: DRUG

KYN-5356, oral tablet

placebo

Intervention Type: DRUG

placebo, oral tablet

Food Effect Cohort

Intervention: KYN-5356 J mg, single dose, oral tablets in fasted or fed state.

Group Type: EXPERIMENTAL

KYN-5356

Intervention Type: DRUG

KYN-5356, oral tablet

Interventions

KYN-5356

KYN-5356, oral tablet

Intervention Type: DRUG

placebo

placebo, oral tablet

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Subject understands the study procedures and agrees to participate by providing written informed consent prior to any study procedures.
• Subject is between 18 and 55 years of age (inclusive), on the date of signing the informed consent form.
• Subject has a body mass index between 18 and 30 kg/m2, inclusive.
• A female subject is eligible to participate if she is not pregnant, not breastfeeding, and at least one of the following conditions applies: Not a woman of childbearing potential or a woman of childbearing potential who agrees to follow the contraceptive guidance (highly effective birth control method) from Screening until end of the study. Note: Males should use appropriate contraceptive method from Screening until end of the study.
• Subject is judged to be in good health by the Principal Investigator based upon the results of a medical history, physical examination, vital signs, 12-lead ECG, and clinical laboratory safety tests.
• Subject is willing to adhere to the study requirements and restrictions.

Exclusion Criteria

• Subject has positive serology for HBsAg, HCV, or HIV, or history of hepatitis from any cause with the exception of hepatitis A that was resolved at least 3 months prior to first dosing of the Investigational Medicinal Product.
• Subject has any illness judged by the Principal Investigator as clinically significant, in the 3 months prior to first dosing of the Investigational Medicinal Product.
• Subject has a suicidality score of "yes" on item 4 or item 5 of the suicidal ideation section of the C-SSRS, if this ideation occurred in the past 6 months, or "yes" on any item of the suicidal behavior section, except for the "Non-Suicidal Self-Injurious Behavior" (item also included in the suicidal behavior section), if this behavior occurred in the past 2 years.
• Subject has a history or current sign or symptom of psychiatric or neurologic disease.
• Subject has a history of head trauma in the past year and/or current seizures.
• Subject is a smoker (use of tobacco products in the previous 3 months from Screening) or uses nicotine or nicotine-containing products and has a positive urine cotinine test at Screening or Admission.
• Subject has a history of alcohol and/or illicit drug abuse within 2 years of entry or has a positive screening test for alcohol and/or drugs of abuse at Screening or Admission.
• Subject consumes caffeine containing beverages exceeding 500 mg caffeine per day (5 cups of coffee) during the off-site days during the study.
• Subject has regular excessive consumption of alcohol within 6 months prior to Screening (7 drinks/week for females, 14 drinks/week for males where 1 drink = 150 mL of wine or 360 mL of beer or 45 mL of hard liquor).
• Subject has a history or current sign or symptom of a cardiovascular, renal, or metabolic bone disease or disease of bone remodeling, or any history of endocrine disease, including an abnormal laboratory result for pre-specified clinical laboratory safety parameters related to these conditions.
• Subject has a history or presence of clinically significant abnormalities detected on 12-lead ECG of either rhythm or conduction. A first-degree atrioventricular block will not be considered as a significant abnormality. Subject has QTcF > 450 ms (mean values per parameter will be considered) detected on the 12-lead ECG at Screening or Admission.
• Presence or sequelae of gastrointestinal, liver, kidney (creatinine clearance <85 mL/min, using the Cockcroft-Gault formula), or other conditions known to interfere with the absorption, distribution, metabolism, or excretion of drugs at Screening or Admission.
• Subject has a history of malignancy within the past 5 years prior to Screening with the exception of excised and curatively treated non-metastatic cell carcinoma of the skin which is considered cured with minimal risk of recurrence.
• Subject tests positive for SARS-CoV-2 at Admission.
• Subject uses any prescription drugs, herbal supplements, within 4 weeks prior to initial dosing, and/or over-the-counter medication, dietary supplements (vitamins included) within 2 weeks prior to initial dosing, other than what is allowed per protocol.
• Subject received vaccination 1 month before admission or plans to receive vaccination during the study.
• Use of other investigational drugs/devices within 5 half-lives of the drug from enrollment (time of the subject signing the informed consent form), or within 30 days, whichever is longer.
• Donation or loss of 400 mL or more of blood within 8 weeks prior to initial dosing.
• Plasma donation (> 200 mL) within 7 days prior to first dosing.
• Resting vital signs at Screening (blood pressure > 140/90 mmHg, heart rate > 90 beats per minute, respiratory rate > 20 breaths per minute, and clinically significant elevated body temperature), or any clinically significant abnormalities in vital signs requiring intervention in the opinion of the Investigator. Up to 2 repeat measurements are permitted to confirm eligibility.

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

Sponsors

Parexel

INDUSTRY

Sponsor Role: collaborator

Kynexis B.V.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Hakop Gevorkyan, MD, MBA

Role: PRINCIPAL_INVESTIGATOR

Parexel

Locations

Parexel Los Angeles Early Phase Clinical Unit

Glendale, California, United States

Countries

United States

Other Identifiers

KYN5356-CL-001

Identifier Type: -

Identifier Source: org_study_id