Clinical trial

A Phase 2 Study of Erdafitinib in Subjects With Advanced Solid Tumors and FGFR Gene Alterations

Name
CR108661
Description
The purpose of this study is to evaluate the efficacy of erdafitinib in terms of overall response rate (ORR) in adult and pediatric participants with advanced solid tumors with fibroblast growth factor receptor (FGFR) alterations (mutations or gene fusions). It will also evaluate ORR in pediatric participants with advanced solid tumors and FGFR alterations.
Trial arms
Trial start
2019-11-20
Estimated PCD
2023-12-04
Trial end
2024-09-20
Status
Active (not recruiting)
Phase
Early phase I
Treatment
Erdafitinib
Participants will receive erdafitinib oral tablets.
Arms:
Erdafitinib
Other names:
JNJ-42756493
Size
316
Primary endpoint
Overall Response Rate (ORR) as Assessed by Independent Review Committee (IRC)
Up to 6 years and 9 months
Eligibility criteria
Inclusion Criteria: * Histologic demonstration of an unresectable, locally advanced, or metastatic solid tumor malignancy with an fibroblast growth factor receptor (FGFR) mutation or FGFR gene fusion * Measurable disease * Participant must have received at least one prior line of systemic therapy in the advanced, unresectable, or metastatic setting; or is a child or adolescent participant with a newly-diagnosed solid tumor and no acceptable standard therapies * Documented progression of disease, defined as any progression that requires a change in treatment, prior to full study screening Exclusion Criteria: * Has had prior chemotherapy, targeted therapy, or treatment with an investigational anticancer agent within 15 days or less than or equal to (\<=) 5 half-lives of the agent (whichever is longer) and up to a maximum of 30 days before the first dose of erdafitinib * The presence of FGFR gatekeeper and resistance mutations * Histologic demonstration of urothelial carcinoma * Hematologic malignancy (i.e., myeloid and lymphoid neoplasms * For non-small cell lung cancer participants only: pathogenic somatic mutations or gene fusions in the following genes: EGFR, ALK, ROS1, NTRK, BRAF V600E and KRAS * Active malignancies other than for disease requiring therapy
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE2'], 'designInfo': {'allocation': 'NA', 'interventionModel': 'SINGLE_GROUP', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'NONE'}}, 'enrollmentInfo': {'count': 316, 'type': 'ACTUAL'}}
Updated at
2024-05-22

1 organization

1 product

5 abstracts

1 indication

Abstract
Efficacy and safety of erdafitinib in pediatric patients with advanced solid tumors and FGFR alterations in the phase 2 RAGNAR trial.
Org: Hopp Children’s Cancer Center Heidelberg (KiTZ), Heidelberg University Hospital and German Cancer Research Center (DKFZ), National Center for Tumor Diseases (NCT), Memorial Sloan Kettering Cancer Center, FLENI,
Abstract
Efficacy and safety of erdafitinib in adults with breast cancer and prespecified fibroblast growth factor receptor alterations in the phase 2 open-label, single-arm RAGNAR trial.
Org: Hospital Privado de la Comunidad de Mar del Plata, Buenos Aires, Argentina, Department of Medical Oncology, West German Cancer Center, University Hospital Essen, Essen, Germany, Vall d’Hebron Barcelona Hospital Campus and Institute of Oncology (VHIO), Barcelona, Spain, Department of Cancer Medicine and INSERM U981, Université Paris-Sud, Université Paris-Saclay, Gustave Roussy, Villejuif, France, Department of Oncology, AK Altona, Asklepios Tumourzentrum Hamburg, Hamburg, Germany,
Abstract
Efficacy and safety of erdafitinib in patients with advanced or metastatic cholangiocarcinoma and FGFR alterations: Pooled analysis of RAGNAR and LUC2001 studies.
Org: The People's Liberation Army 81 Hospital, University Hospital Gasthuisberg, Bristol Haematology and Oncology Centre, Statistics & Decision Sciences, Janssen China R&D Center, Chi-Mei Medical Center,
Abstract
Efficacy and safety of erdafitinib in adults with NSCLC and prespecified fibroblast growth factor receptor alterations in the phase 2 open-label, single-arm RAGNAR trial.
Org: Department of Medical Oncology, West German Cancer Center, University Hospital Essen, Essen, Germany, Vall d'Hebron University Hospital and Institute of Oncology (VHIO), Barcelona, Spain, Hospital Privado de la Comunidad de Mar del Plata, Buenos Aires, Argentina, Department of Cancer Medicine, INSERM U981, Gustave Roussy, Université Paris-Saclay, Villejuif, France, The University of Texas MD Anderson Cancer Center, Houston, TX, USA,
Abstract
Tumor agnostic efficacy and safety of erdafitinib (erda) in patients (pts) with advanced solid tumors with prespecified FGFR alterations (FGFRalt): RAGNAR primary analysis.
Org: Janssen Research & Development, Beerse, PA, Belgium, Janssen Research & Development, Shanghai City, China, Janssen Research & Development, Spring House, PA,