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A Phase 1 Study to Evaluate the Pharmacokinetics of JDQ443 in Participants With Hepatic Impairment Compared to Matched Healthy Control Participants.

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Novartis

Status and phase

Terminated
Phase 1

Conditions

Small Cell Lung Carcinoma

Treatments

Drug: JDQ443

Study type

Interventional

Funder types

Industry

Identifiers

NCT05329623
CJDQ443B12103

Details and patient eligibility

About

The purpose of this study is to evaluate the effect of hepatic impairment on the systemic pharmacokinetics (PK), safety, and tolerability of JDQ443 in participants with varying degrees of hepatic impairment.

Full description

This is a Phase 1, open-label, single-dose, multi-center, parallel group study to evaluate the PK of oral JDQ443 in participants with mild, moderate, and/or severe hepatic impairment compared to matched healthy control participants.

The study comprises a 28-day Screening period (Days -28 to -2), a baseline evaluation period (Day -1), a single dose administration of 200 mg of JDQ443 (Day 1), and a follow-up period of 4 days (Days 2 to 4) for PK sample collection. All participants should have a post-study safety follow-up contact conducted approximately 30 days after last administration of study treatment. The study will be considered complete once all the participants have finished the required assessments or have dropped out or been lost to follow-up.

A total of up to 48 participants will be enrolled in this study. Approximately 8 participants will be enrolled in each of mild (Child-Pugh A; Group 2), moderate (Child-Pugh B; Group 3), and severe (Child-Pugh C; Group 4) hepatic impairment groups (to have at least six evaluable participants in each group). Each participant in the healthy control group (Group 1) will be matched to one or more evaluable participants with hepatic impairment with respect to age, body weight and sex. All participants will receive a single JDQ443 dose. Upon completion of mild and moderate impairment groups, as well as matching control participants, an interim analysis will be conducted to compare the PK exposure of the two hepatic impaired groups (Groups 2 and 3) to that of the control participants. The interim analysis is to mitigate the potential safety risks in participants with severe hepatic impairment. If the interim analysis results do not show a clinically relevant increase in exposure of JDQ443 and is well tolerated from a safety perspective, then severe hepatic impairment participants may be enrolled. Participants with severe hepatic impairment will be enrolled only after the completion of the interim analysis.

Enrollment

33 patients

Sex

All

Ages

18 to 75 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Key inclusion Criteria:

  • Written informed consent must be obtained before any assessment is performed.
  • Participants must weigh at least 50.0 kg to participate in the study and must have a body mass index (BMI) within the range of 18 to 40 kg/m2.
  • Ability to communicate well with the investigator, to understand and comply with the requirements of the study.
  • Participant must be willing to remain in the clinical research unit as required by the protocol.

Key exclusion Criteria:

  • Use of other investigational drugs within the last 30 days or 5 half-lives prior to dosing, whichever is longer.
  • Use of drugs (prescription, non-prescription and herbal remedies such as St John's wort) known to affect cytochrome p (CYP)3A, including both strong and moderate inhibitors and inducers, within 2 weeks prior to dosing until completion of the EOS Visit.
  • Contradiction or hypersensitivity to the investigational compound/compound class or its excipients being used in this study.
  • Pregnant or nursing (lactating) women. Pregnancy is defined as the state of a female after conception and until termination of gestation, confirmed by a positive human chorionic gonadotropin (hCG) laboratory test.
  • Known history of, or current clinically significant arrhythmias, history of prolonged QT correction formula (QTcF) interval or QTcF >480 msec

Other inclusion/exclusion criteria may apply

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

33 participants in 4 patient groups

Normal hepatic function
Experimental group
Description:
Matched healthy participants with normal hepatic function
Treatment:
Drug: JDQ443
Mild hepatic impairment
Experimental group
Description:
Mild hepatic impaired participants with Child-Pugh A (score of 5 to 6)
Treatment:
Drug: JDQ443
Moderate hepatic impairment
Experimental group
Description:
Moderate hepatic impairment with Child Pugh B (score from 7 to 9)
Treatment:
Drug: JDQ443
Severe hepatic impairment
Experimental group
Description:
Severe hepatic impairment with Child Pugh C (score from 10 to 15)
Treatment:
Drug: JDQ443

Trial contacts and locations

2

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Central trial contact

Novartis Pharmaceuticals; Novartis Pharmaceuticals

Data sourced from clinicaltrials.gov

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