Rucaparib Hepatic Impairment Study in Patients With a Solid Tumor

NCT ID: NCT03521037

Last Updated: 2023-06-09

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 16 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2018-02-27
• Study Completion Date: 2021-02-24

Brief Summary

Phase 1, open-label, parallel group, PK, safety and tolerability study in patients with an advanced solid tumor and either normal hepatic function (Group 1, n = 8) or moderate hepatic impairment (Group 2, n = 8) according to the NCI-ODWG criteria. Patients in Group 1 and Group 2 may be enrolled in parallel, with preferential enrollment of Group 2 patients before Group 1 patients. The study will consist of 2 parts: a single-dose PK part (Part I) and a continuous rucaparib treatment part (Part II).

Detailed Description

In Part I, eligible patients will receive a single oral dose of 600 mg rucaparib followed by intensive plasma PK sampling up to Day 7 (hour 144). In Part II, patients may continue to receive continuous oral rucaparib in 28 day cycles. The starting dose for all Group 1 patients will be 600 mg BID. The first 2 patients with moderate hepatic impairment (Group 2) that enter Part II will receive a starting dose of 400 mg BID rucaparib; a lower dose of rucaparib may also be set based on PK results observed in Part I. If this initial starting dose is determined to be safe and tolerable as determined by real-time PK data and dose limiting toxicities (DLT) observed during the first 28 days of rucaparib, the starting dose of rucaparib may be increased in subsequent Group 2 patients. The starting dose for Group 2 patients may also be lowered, based on the patients' real time PK and emerging safety data. The Sponsor and key clinical research organization (CRO) staff will review available adverse event, laboratory, and PK data to determine the starting dose for subsequent Group 2 patients, as well as allowing intra-patient dose escalation of rucaparib after Cycle 1.Treatment with rucaparib will continue until progression of disease, unacceptable toxicity, death, loss to follow-up, withdrawal of consent, or other appropriate clinical reason for discontinuation.

Conditions

Neoplasms

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: OTHER
• Blinding Strategy: NONE

Study Groups

no name

Group 1: patients with normal hepatic function Group 2: patients who have moderate hepatic impairment

Group Type: EXPERIMENTAL

Rucaparib camsylate

Intervention Type: DRUG

In Part I, eligible patients will receive a single oral dose of 600 mg rucaparib followed by intensive plasma PK sampling up to Day 7 (hour 144). In Part II, patients may continue to receive continuous oral rucaparib in 28 day cycles.

Interventions

Rucaparib camsylate

In Part I, eligible patients will receive a single oral dose of 600 mg rucaparib followed by intensive plasma PK sampling up to Day 7 (hour 144). In Part II, patients may continue to receive continuous oral rucaparib in 28 day cycles.

Intervention Type: DRUG

Other Intervention Names

rubraca

Eligibility Criteria

Inclusion Criteria

All Patients:

• Patients ≥18 years of age at the time the ICF is signed;
• Patients with a histologically or cytologically confirmed advanced solid tumor who, in the opinion of the Investigator, could potentially benefit from treatment with rucaparib
• ECOG PS less than or equal to 2
• Adequate bone marrow and renal function

Hepatically Impaired Patients (in addition):

• Stable hepatic impairment as judged by the Investigator
• Moderate Hepatic Impairment (NCI-ODWG criteria) during Screening

Patients with Normal Hepatic Function (in addition):

• Normal Hepatic Function (NCI-ODWG criteria)

Exclusion Criteria

All Patients:

• Prior treatment with chemotherapy, radiation, antibody therapy or other immunotherapy, gene therapy, vaccine therapy, angiogenesis inhibitors, or investigational drugs within 14 days prior to day 1
• Ongoing toxicity ≥ Grade 2 per Common Terminology Criteria for Adverse Events criteria (CTCAE version 4.03)
• Prior treatment with any poly adenosine diphosphate ribose polymerase inhibitor
• Arterial or venous thrombi (including cerebrovascular accident), myocardial infarction, admission for unstable angina, cardiac angioplasty, stenting or poorly controlled hypertension within the last 3 months prior to Screening
• Pre-existing duodenal stent, and/or any gastrointestinal disorder or defect that would, in the opinion of the Investigator, interfere with absorption of rucaparib
• Hospitalization for bowel obstruction within 3 months prior to Day 1
• Untreated or symptomatic central nervous system (CNS) metastases
• Evidence or history of bleeding disorder
• Acute illness within 14 days prior to Day 1
• Active second malignancy

Hepatically Impaired Patients (in addition):

• Severe hepatic encephalopathy (Grade >2);
• History of liver transplantation;
• Advanced ascites or ascites that require drainage and albumin supplementation, as judged by the Investigator;
• Acute damage of the liver with Grade 4 AST/ALT values

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

pharmaand GmbH

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Wojewódzki Szpital Specjalistyczny w Białej Podlaskiej

Biała Podlaska, , Poland

Med Polonia Sp. z o.o.

Poznan, , Poland

Zachodniopomorskie Centrum Onkologii w Szczecinie

Szczecin, , Poland

BioVirtus Centrum Medyczne

Warsaw, , Poland

Summit Clinical Research s.r.o.

Bratislava, , Slovakia

Northern Centre for Cancer Care

Newcastle upon Tyne, , United Kingdom

Countries

Poland; Slovakia; United Kingdom

Other Identifiers

CO-338-078

Identifier Type: -

Identifier Source: org_study_id