A Phase 1, Open-label, Multi-center, Single-dose, Parallel Group Study to Evaluate the Pharmacokinetics of Siremadlin (HDM201) in Participants With Mild, Moderate and Severe Hepatic Impairment Compared to Matched Healthy Control Participants

Novartis Pharmaceuticals3 sites in 1 country38 target enrollmentDecember 2, 2022

ConditionsHepatic Impairment

InterventionsSiremadlin

DrugsSiremadlin

Overview

Phase: Phase 1
Intervention: Siremadlin
Conditions: Hepatic Impairment
Sponsor: Novartis Pharmaceuticals
Enrollment: 38
Locations: 3
Primary Endpoint: Pharmacokinetics (PK): Tlast
Status: Completed
Last Updated: 9 months ago

Overview Investigators Eligibility Criteria Arms & Interventions Outcomes Sites Similar Trials

Overview

Brief Summary

The main purpose of this study is to evaluate the effect of varying degrees of impaired hepatic function (by Child Pugh classification) on the plasma PK of siremadlin after a single oral dose. In addition, safety and tolerability of siremadlin after a single oral dose will be evaluated. The results of this study will inform the decision whether a dose adjustment may be recommended when treating patients with various degrees of impaired hepatic function.

Detailed Description

Participants will be recruited into one of 4 groups according to the Child-Pugh classification score. Participants with HI will be enrolled into either mild (Child-Pugh A; Group 2), moderate (Child Pugh B; Group 3) or severe (Child-Pugh C; Group 4) HI groups. Healthy control participants (Group 1) will be matched to 1 or more participants with HI with respect to age (± 10 years), body weight (± 20%) and sex. Each participant in the matched healthy control group (Group 1) can be matched to participant(s) in any HI group (Groups 2, 3, and 4). The study will enroll the four groups in parallel. Therefore, enrollment in Group 1 will remain open until enrollment in the mild, moderate and severe HI groups is complete and each HI participant has a matched healthy control (Group 1) participant. Participants from Group 1 will be enrolled after at least 3 participants from each of Groups 2 and 3 have completed all scheduled assessments. The study consists of a screening period of up to 28 days (Days -29 to -2), a baseline evaluation on Day -1, a single dose administration of siremadlin on Day 1 followed by PK sampling up to 144 hours post-dose (Day 7). All baseline safety evaluation results must be available and reviewed prior to the dosing. All eligible participants will be domiciled from Day -1 until Day 7. Safety assessments will include physical examinations, ECGs, vital signs, standard clinical laboratory evaluations (hematology, blood chemistry, urinalysis, coagulation), AE and serious adverse event (SAE) monitoring. All participants will have a post-study safety follow-up contact conducted approximately 30 days after administration of study treatment. The study will be considered complete once all the participants have finished the required assessments, dropped out, or been lost to follow-up before completing the required assessments. The total study duration for each participant is expected to be up to maximum of 59 days, including the Screening period and the 30-day post-study safety contact follow up period.

Registry

clinicaltrials.gov

Start Date

December 2, 2022

End Date

September 18, 2023

Last Updated

9 months ago

Study Type

Interventional

Study Design

Parallel

Sex

All

Investigators

Sponsor

Novartis Pharmaceuticals

Responsible Party

Sponsor

Eligibility Criteria

Inclusion Criteria

•All participants:
•Male and non-child-bearing potential females between 18 and 75 years of age, inclusive, at Screening.
•Participant must have been a non-smoker or moderate smoker (up to 10 cigarettes or equivalent nicotine containing products per day) at Screening. Participant must have agreed to maintain the same smoking status (i.e., smoker or non-smoker) from Screening until after Study Completion evaluations.
•Additional key inclusion criteria for healthy participants (Group 1):
•Participants must have weighed at least 50.0 kg and must have had a BMI within the range of 18.0 to 38.0 kg/m2, inclusive at Screening.
•Participants with no clinically significant abnormalities as determined by past medical history, physical examination, ECG and clinical laboratory test at Screening.
•Additional inclusion criteria for mild, moderate and severe HI participants (Groups 2-4):
•Participants must have weighed at least 50.0 kg and must have had a BMI within the range of 18.0 to 38.0 kg/m2, inclusive at Screening. For participants without overt ascites, the BMI must have been within the range of 18.0 to 40.0 kg/m2, inclusive. For participants with overt ascites, the BMI must have been within the range of 18.0 to 45.0 kg/m2, inclusive.
•Participant must have satisfied the criteria for HI as evidenced by a Child-Pugh class of A, B, or C at Screening and Baseline (see Table 8-2 Child-Pugh classification criteria):
•Group 2: Class A; Mild; Child-Pugh score 5-6, inclusive

Exclusion Criteria

•All participants (Groups 1-4):
•Contraindication or hypersensitivity to the investigational compound/compound class or excipients being used in this study.
•History or presence of clinically significant ECG abnormalities or a family history or presence of prolonged QT-interval syndrome.
•History of malignancy of any organ system, treated or untreated, within 3 years prior to Screening, regardless of whether there were recurrence or metastases. Those with localized basal cell carcinoma of the skin, in-situ cervical cancer, or hepatocellular cancer treated with local ablative therapy more than 6 months prior to Screening may have been enrolled.
•Use of investigational drugs, other than siremadlin (i.e., participation in any clinical investigation) within 4 weeks prior to dosing or longer if required by local regulation, or within 5 half-lives of the investigational agent taken prior to dosing (whichever was longer).
•Clinically significant illness within 2 weeks prior to dosing that may have jeopardized safety of the study participant and/or alter the study results as judged by the Investigator.
•Additional key exclusion criteria for healthy participants (Group 1):
•Any single parameter of ALT, AST, GGT, or ALP that exceeded 1.2 x ULN or ≥ 1.5 x ULN TBL or any elevation above ULN of more than one parameter of ALT, AST, GGT, ALP, or serum TBL at Screening.
•Participants known to have Gilbert's syndrome.
•Participants with abnormal laboratory values for the following parameters at Screening:

Arms & Interventions

Group 1: Healthy Control

Each healthy participant will receive a single dose of HDM201

Intervention: Siremadlin

Group 2: Mild; Child-Pugh A

Each participant with mild Child-Pugh will receive a single dose of HDM201

Intervention: Siremadlin

Group 3: Moderate; Child-Pugh B

Each participant with moderate Child-Pugh will receive a single dose of HDM201

Intervention: Siremadlin

Group 4: Severe; Child-Pugh C

Each participant with severe Child-Pugh will receive a single dose of HDM201

Intervention: Siremadlin