Phase 1 Study of the Combination of Rogaratinib With Copanlisib in Patients With Fibroblast Growth Factor Receptor (FGFR)-Positive, Locally Advanced or Metastatic Solid Tumors

NCT ID: NCT03517956

Last Updated: 2022-07-14

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 16 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2018-07-25
• Study Completion Date: 2021-02-01

Brief Summary

The primary objective of this study is to determine the safety, tolerability, maximum tolerated dose (MTD) or recommended Phase 2 dose (RP2D) and efficacy of rogaratinib in combination with copanlisib in patients with locally advanced or metastatic solid tumors that are mRNA-positive for at least one FGFR1-4 subtype.

The secondary objectives of this study are to characterize the pharmacokinetics (PK) of rogaratinib and copanlisib alone and in combination, and to assess the anti-tumor efficacy of rogaratinib in combination with copanlisib for locally advanced or metastatic solid tumors that are mRNA-positive for at least one FGFR1-4 subtype.

Conditions

Advanced or Metastatic Solid Tumor

Study Design

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

Study Groups

Patients with FGFR1-4 - positive solid tumors

Dose escalation:

The starting dose of the combination will be escalated in a stepwise fashion, escalating one drug at a time.

Dose expansion (urothelial cancer):

Patients in the dose expansion will be treated with the combination identified in the dose escalation part of the study.

Group Type: EXPERIMENTAL

Rogaratinib (BAY1163877)

Intervention Type: DRUG

Dose escalation:

Starting dose is rogaratinib 400 mg twice daily (b.i.d.) in continuous 28-day cycles from Cycle 1 Day 3 onwards.

Dose expansion:

With dose identified in dose escalation part.

Copanlisib (BAY80-6946)

Intervention Type: DRUG

Dose escalation:

Starting dose is 45 mg on Days 1, 8 and 15 of each 28-day cycle.

Dose expansion:

With dose identified in dose escalation part.

Interventions

Rogaratinib (BAY1163877)

Dose escalation:

Starting dose is rogaratinib 400 mg twice daily (b.i.d.) in continuous 28-day cycles from Cycle 1 Day 3 onwards.

Dose expansion:

With dose identified in dose escalation part.

Intervention Type: DRUG

Copanlisib (BAY80-6946)

Dose escalation:

Starting dose is 45 mg on Days 1, 8 and 15 of each 28-day cycle.

Dose expansion:

With dose identified in dose escalation part.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• High FGFR mRNA expression levels (RNAscope score of ≥3; measurement is part of this protocol) in archival or fresh tumor biopsy specimen.
• Eastern Cooperative Oncology Group Performance Status (ECOG PS) of 0 or 1.
• At least 1 measurable lesion according to Response Evaluation Criteria in Solid Tumors (RECIST 1.1) in contrast enhanced (unless contraindicated) CT or MRI.
• Adequate bone marrow, liver and renal function.
• Glomerular filtration rate (GFR) ≥ 30 mL/min/1.73 m*2 according to the Modification of Diet in Renal Disease (MDRD) formula.
• Left ventricular ejection fraction (LVEF) equal to or above the lower limit of normal (LLN) at the institution.
• Life expectancy of at least 3 months.
• For the dose escalation part: Patients with histologically confirmed, locally advanced or metastatic solid tumors who are not candidates for or refuse standard therapy or whose disease progressed and for which standard anti-cancer treatment is no longer effective, excluding primary brain or spinal tumors. Patients who have been advised with all standard treatment options and still refuse them must be documented and can be allowed to enter the trial.
• For the dose expansion part: Patients with histologically confirmed, locally advanced or metastatic urothelial carcinoma (transitional cell carcinoma) including urinary bladder, renal pelvis, ureters, urethra who are not candidates for or refuse standard therapy or whose disease progressed and for which standard anticancer treatment is no longer effective. Patients who have been advised with all standard treatment options and still refuse them must be documented and can be allowed to enter the trial.

Exclusion Criteria

• Previous or concurrent cancer that is distinct from tumor for which the patient is enrolled in the study, except

• curatively treated cervical carcinoma in situ
• treated basal-cell carcinoma
• localized prostate cancer treated with curative intent and known absence of prostate-specific antigen (PSA) relapse or incidental prostate cancer (T1/T2a, Gleason score ≤ 6, and PSA ≤ 10 ng/mL undergoing active surveillance and treatment-naïve)
• any cancer curatively treated > 3 years before planned start of study treatment.
• Ongoing or previous anti-cancer treatment within 4 weeks of study treatment start (or 6 weeks for mitomycin C, nitrosoureas and monoclonal antibodies); with exceptions.
• Prior toxicity to anti-FGFR-directed or anti-PI3K-directed therapies leading to treatment discontinuation (previous exposure is allowed in other circumstances). If prior toxicity to anti-FGFR-directed or anti-PI3K-directed therapies leading to treatment discontinuation is different from the known safety profile of rogaratinib or copanlisib, enrollment is allowed.
• Symptomatic brain or meningeal metastatic tumors unless the patient is >6 months from definitive therapy, has no evidence of tumor growth on an imaging study and is clinically stable with respect to the tumor at the start of study treatment. Also the patient must not be undergoing acute steroid therapy or taper (chronic steroid therapy is acceptable provided that the dose is stable for one month prior to and following screening radiographic studies).
• History or current condition of an uncontrolled cardiovascular disease including congestive heart failure NYHA > Class 2, unstable angina (symptoms of angina at rest) or new-onset angina (within last 3 months) or myocardial infarction within past 6 months and cardiac arrhythmias requiring anti-arrhythmic therapy (beta-blockers or digoxin are permitted).
• Active hepatitis B (HBV) or C (HCV) infection.
• Active clinically serious infections (≥ CTCAE v4.03 Grade 2).

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

Sponsors

Bayer

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

USC Norris Hospital and Clinics

Los Angeles, California, United States

Northwestern University

Chicago, Illinois, United States

University of Maryland

Baltimore, Maryland, United States

Dana-Farber Cancer Institute

Boston, Massachusetts, United States

Barbara Ann Karmanos Cancer Institute - Detroit

Detroit, Michigan, United States

Memorial Sloan-Kettering Cancer Center

New York, New York, United States

Tyler Cancer Center

Tyler, Texas, United States

CU Saint-Luc/UZ St-Luc

Bruxelles - Brussel, , Belgium

UZ Antwerpen

Edegem, , Belgium

CHU de Liège

Liège, , Belgium

Krankenhaus Nordwest

Frankfurt am Main, Hesse, Germany

Universitätsklinikum Köln

Cologne, North Rhine-Westphalia, Germany

Klinikum der Universität Würzburg

Würzburg, , Germany

National University Hospital

Singapore, , Singapore

National Cancer Center Singapore

Singapore, , Singapore

Severance Hospital, Yonsei University Health System

Seoul, , South Korea

Asan Medical Center

Seoul, , South Korea

Samsung Medical Center

Seoul, , South Korea

Ciutat Sanitària i Universitaria de la Vall d'Hebron

Barcelona, , Spain

Hospital Clínico Universitario de Valencia

Valencia, , Spain

Countries

United States; Belgium; Germany; Singapore; South Korea; Spain

Other Identifiers

2018-000419-26

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

19774

Identifier Type: -

Identifier Source: org_study_id