Success Metrics

Clinical Success Rate
25.0%

Based on 2 completed trials

Completion Rate
25%(2/8)
Active Trials
8(42%)
Results Posted
350%(7 trials)
Terminated
6(32%)

Phase Distribution

Ph phase_3
4
21%
Ph phase_1
4
21%
Ph phase_2
11
58%

Phase Distribution

4

Early Stage

11

Mid Stage

4

Late Stage

Phase Distribution19 total trials
Phase 1Safety & dosage
4(21.1%)
Phase 2Efficacy & side effects
11(57.9%)
Phase 3Large-scale testing
4(21.1%)

Highest Phase Reached

Phase 3

Trial Status & Enrollment

Completion Rate

25.0%

2 of 8 finished

Non-Completion Rate

75.0%

6 ended early

Currently Active

8

trials recruiting

Total Trials

19

all time

Status Distribution
Active(11)
Completed(2)
Terminated(6)

Detailed Status

Recruiting6
Terminated6
Not yet recruiting3
Completed2
Active, not recruiting2

Development Timeline

Analytics

Development Status

Total Trials
19
Active
8
Success Rate
25.0%
Most Advanced
Phase 3

Trials by Phase

Phase 14 (21.1%)
Phase 211 (57.9%)
Phase 34 (21.1%)

Trials by Status

not_yet_recruiting316%
completed211%
recruiting632%
active_not_recruiting211%
terminated632%

Recent Activity

Clinical Trials (19)

Showing 19 of 19 trials
NCT07745296Phase 3

Investigating Precision Medicine in the Adjuvant Setting in Biliary Tract Cancer

Not Yet Recruiting
NCT06506955Phase 2

Futibatinib in Patients Previously Enrolled in an Antecedent Futibatinib as Monotherapy or Combination Therapy.

Active Not Recruiting
NCT07710885Phase 3

Futibatinib (TAS-120) in Patients With Advanced Biliary Tract Cancer

Recruiting
NCT02813135Phase 1

European Proof-of-Concept Therapeutic Stratification Trial of Molecular Anomalies in Relapsed or Refractory Tumors

Recruiting
NCT07639528Phase 2

Preoperative Durvalumab, Cisplatin, Gemcitabine With or Without Futibatinib Targeted Therapy for the Treatment of Resectable Intrahepatic Cholangiocarcinoma, OPTIC Trial

Not Yet Recruiting
NCT05827614Phase 1

Study of the CHK1 Inhibitor BBI-355, an ecDNA-directed Therapy (ecDTx), and the RNR Inhibitor BBI-825, in Subjects With Tumors With Oncogene Amplifications

Terminated
NCT02693535Phase 2

TAPUR: Testing the Use of Food and Drug Administration (FDA) Approved Drugs That Target a Specific Abnormality in a Tumor Gene in People With Advanced Stage Cancer

Recruiting
NCT05615818Phase 3

Personalized Medicine for Advanced Biliary Cancer Patients

Recruiting
NCT07594548Phase 1

Futibatinib With Paclitaxel and Ramucirumab for the Treatment of Locally Advanced or Unresectable Gastric, Gastroesophageal Junction, or Esophageal Adenocarcinoma

Not Yet Recruiting
NCT05945823Phase 2

Phase 2 Futibatinib in Combination With PD-1 Antibody Based Standard of Care in Solid Tumors

Active Not Recruiting
NCT05036681Phase 2

A Phase II Study of Futibatinib and Pembrolizumab in Metastatic Microsatellite Stable Endometrial Carcinoma

Terminated
NCT04601857Phase 2

Futibatinib and Pembrolizumab Combination in the Treatment of Advanced or Metastatic Urothelial Carcinoma

Terminated
NCT06263153Phase 2

Futibatinib in Combination With Durvalumab Prior to Cystectomy for the Treatment of Muscle-Invasive Bladder Cancer Patients Who Are Ineligible for Cisplatin-based Therapy

Recruiting
NCT04828486Phase 2

Futibatinib and Pembrolizumab for Treatment of Advanced or Metastatic FGF19 Positive BCLC Stage A, B, or C Liver Cancer

Completed
NCT04024436Phase 2

A Study of TAS-120 in Patients With Metastatic Breast Cancer

Terminated
NCT04189445Phase 2

Futibatinib in Patients With Specific FGFR Aberrations

Terminated
NCT02052778Phase 1

A Study of TAS-120 in Patients With Advanced Solid Tumors

Completed
NCT04093362Phase 3

Futibatinib Versus Gemcitabine-Cisplatin Chemotherapy as First-Line Treatment of Patients With Advanced Cholangiocarcinoma Harboring FGFR2 Gene Rearrangements

Terminated
NCT03767075Phase 2

A Modular Multi-Basket Trial to Improve Personalized Medicine in Cancer Patients (Basket of Baskets)

Recruiting

All 19 trials loaded

Drug Details

Intervention Type
DRUG
Total Trials
19