Register a trial

Registering a new trial?

To achieve prospective registration, we recommend submitting your trial for registration at the same time as ethics submission.

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been endorsed by the ANZCTR. Before participating in a study, talk to your health care provider and refer to this information for consumers
Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT03834220




Registration number
NCT03834220
Ethics application status
Date submitted
4/02/2019
Date registered
7/02/2019

Titles & IDs
Public title
Basket Trial in Solid Tumors Harboring a Fusion of FGFR1, FGFR2 or FGFR3- (FUZE Clinical Trial)
Scientific title
A Phase II Basket Study of the Oral Selective Pan-FGFR Inhibitor Debio 1347 in Subjects With Solid Tumors Harboring a Fusion of FGFR1, FGFR2 or FGFR3
Secondary ID [1] 0 0
2018-003584-53
Secondary ID [2] 0 0
Debio 1347-201
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Solid Tumor 0 0
Condition category
Condition code

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Drugs - Debio 1347

Experimental: Cohort 1: Debio 1347 (Biliary Tract Cancer) - Participants with biliary tract cancer were included in this cohort to receive Debio 1347 80 milligrams (mg) tablets, orally, once daily (QD), from Day 1 to Day 28 in 28-day cycles until the occurrence of disease progression or unacceptable toxicity (up to a median duration of 20 weeks).

Experimental: Cohort 2: Debio 1347 (Urothelial Cancer) - Participants with urothelial cancer were included in this cohort to receive Debio 1347 80 mg tablets, orally, QD, from Day 1 to Day 28 in 28-day cycles until the occurrence of disease progression or unacceptable toxicity (up to a median duration of 5.86 weeks).

Experimental: Cohort 3: Debio 1347 (All Other Solid Tumor Histologies) - Participants with all other solid tumor histologies were included in this cohort to receive Debio 1347 80 mg tablets, orally, QD, from Day 1 to Day 28 in 28-day cycles until the occurrence of disease progression or unacceptable toxicity (up to a median duration of 8.14 weeks).


Treatment: Drugs: Debio 1347
Debio 1347 oral tablets.
Intervention code [1] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Objective Response Rate (ORR) as Centrally Measured by Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST 1.1) Criteria
Timepoint [1] 0 0
Up to disease progression or end of study (up to 1 year and 9 months)
Secondary outcome [1] 0 0
Duration of Response (DOR) as Centrally Measured by Independent Review Committee (IRC)
Timepoint [1] 0 0
Up to disease progression or end of study (up to 2 years and 9 months)
Secondary outcome [2] 0 0
Disease Control Rate (DCR) as Centrally Measured by Independent Review Committee (IRC)
Timepoint [2] 0 0
Up to disease progression or end of study (up to 2 years and 9 months)
Secondary outcome [3] 0 0
Progression-Free Survival (PFS) as Centrally Measured by Independent Review Committee (IRC)
Timepoint [3] 0 0
From the start of the study up to disease progression or death (up to 2 years and 9 months)
Secondary outcome [4] 0 0
Overall Survival (OS)
Timepoint [4] 0 0
Until death or loss to follow-up or end of study (up to 2 years and 9 months)
Secondary outcome [5] 0 0
Number of Participants With Treatment-Emergent Adverse Events (TEAEs) Assessed by National Cancer Institute Common Terminology Criteria (NCI CTCAE) v5.0 and Serious Adverse Events (SAEs)
Timepoint [5] 0 0
From first dose of study drug up to 30 days post last dose (Up to 2 years and 9 months)
Secondary outcome [6] 0 0
Trough Concentration at Steady State (Ctrough,ss) of Debio 1347 in Plasma
Timepoint [6] 0 0
Predose and post dose up to Cycle 2 Day 28 (each cycle length = 28 days)
Secondary outcome [7] 0 0
Area Under the Plasma Concentration-Time Curve Over the Dosing Interval at Steady State (AUCtau,ss) of Debio 1347 in Plasma
Timepoint [7] 0 0
Predose and post dose up to Cycle 2 Day 28 (each cycle length = 28 days)
Secondary outcome [8] 0 0
Correlation of Debio 1347 Plasma Concentration (C) and QT Interval Corrected for Heart Rate Using Fridericia's Formula (QTcF)
Timepoint [8] 0 0
Pre-dose on Days 14 and 28, and 1, 3, 7 hours post-dose on Day 28 of Cycle 1; pre-dose on Days 14 and 28, and 3 hours post-dose on Day 28 of Cycle 2 (each cycle length = 28 days)

Eligibility
Key inclusion criteria
* Cytologically or histologically confirmed advanced solid tumor
* Radiographic progression on prior systemic therapy; prior localized therapy (i.e., radiation, ablation, embolization) is allowed provided radiographic progression out-of-field or in the treatment, field is shown
* Locally-advanced (unresectable) or metastatic disease harboring an FGFR1-3 gene fusion/rearrangement potentially leading to a functional FGFR aberrant protein, identified through local and/or central molecular assay
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
* History of hypersensitivity to any of the excipients in the Debio 1347 formulation
* History and/or current evidence of ectopic mineralization/calcification, including but not limited to soft tissue, kidneys, intestine, myocardia, or lung, excepting calcified lymph nodes, lung nodules and asymptomatic vascular or cartilage/tendon calcifications
* Administration of any investigational agent within 2 weeks prior to initial dosing with Debio 1347 (3 weeks for immune checkpoint inhibitors)

Study design
Purpose of the study
Treatment
Allocation to intervention
Non-randomised trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Parallel
Other design features
Phase
Phase 2
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Stopped early
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
22/03/2019
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
4/01/2022
Sample size
Target
Accrual to date
Final
63
Recruitment in Australia
Recruitment state(s)
Recruitment hospital [1] 0 0
Southern Highlands Private Hospital - Bowral
Recruitment hospital [2] 0 0
Peninsula and Southeast Oncology (PASO) - Frankston
Recruitment hospital [3] 0 0
Linear Clinical Research, B Block Sir Charles Gairdner Hospital - Nedlands
Recruitment hospital [4] 0 0
John Flynn Private Hospital - Tugun
Recruitment postcode(s) [1] 0 0
NSW 2576 - Bowral
Recruitment postcode(s) [2] 0 0
3199 - Frankston
Recruitment postcode(s) [3] 0 0
6009 - Nedlands
Recruitment postcode(s) [4] 0 0
4224 - Tugun
Recruitment outside Australia
Country [1] 0 0
United States of America
State/province [1] 0 0
Arizona
Country [2] 0 0
United States of America
State/province [2] 0 0
California
Country [3] 0 0
United States of America
State/province [3] 0 0
Florida
Country [4] 0 0
United States of America
State/province [4] 0 0
Kentucky
Country [5] 0 0
United States of America
State/province [5] 0 0
Louisiana
Country [6] 0 0
United States of America
State/province [6] 0 0
Maryland
Country [7] 0 0
United States of America
State/province [7] 0 0
Massachusetts
Country [8] 0 0
United States of America
State/province [8] 0 0
Michigan
Country [9] 0 0
United States of America
State/province [9] 0 0
New Jersey
Country [10] 0 0
United States of America
State/province [10] 0 0
New York
Country [11] 0 0
United States of America
State/province [11] 0 0
North Carolina
Country [12] 0 0
United States of America
State/province [12] 0 0
Ohio
Country [13] 0 0
United States of America
State/province [13] 0 0
Oklahoma
Country [14] 0 0
United States of America
State/province [14] 0 0
Pennsylvania
Country [15] 0 0
United States of America
State/province [15] 0 0
Texas
Country [16] 0 0
United States of America
State/province [16] 0 0
Utah
Country [17] 0 0
United States of America
State/province [17] 0 0
Washington
Country [18] 0 0
United States of America
State/province [18] 0 0
Wisconsin
Country [19] 0 0
Austria
State/province [19] 0 0
Salzburg
Country [20] 0 0
Austria
State/province [20] 0 0
Wiener Neustadt
Country [21] 0 0
Brazil
State/province [21] 0 0
Ijuí
Country [22] 0 0
Brazil
State/province [22] 0 0
Rio Grande
Country [23] 0 0
Brazil
State/province [23] 0 0
Santo André
Country [24] 0 0
Brazil
State/province [24] 0 0
São Paulo
Country [25] 0 0
Bulgaria
State/province [25] 0 0
Dobrich
Country [26] 0 0
Bulgaria
State/province [26] 0 0
Plovdiv
Country [27] 0 0
Bulgaria
State/province [27] 0 0
Sofia
Country [28] 0 0
Croatia
State/province [28] 0 0
Varaždin
Country [29] 0 0
Croatia
State/province [29] 0 0
Zagreb
Country [30] 0 0
Czechia
State/province [30] 0 0
Brno
Country [31] 0 0
Czechia
State/province [31] 0 0
Hradec Králové
Country [32] 0 0
Czechia
State/province [32] 0 0
Olomouc
Country [33] 0 0
Czechia
State/province [33] 0 0
Prague
Country [34] 0 0
Czechia
State/province [34] 0 0
Praha
Country [35] 0 0
Denmark
State/province [35] 0 0
Aalborg
Country [36] 0 0
Denmark
State/province [36] 0 0
Herlev
Country [37] 0 0
Denmark
State/province [37] 0 0
Odense
Country [38] 0 0
Finland
State/province [38] 0 0
Helsinki
Country [39] 0 0
France
State/province [39] 0 0
Angers
Country [40] 0 0
France
State/province [40] 0 0
Bordeaux
Country [41] 0 0
France
State/province [41] 0 0
Lille
Country [42] 0 0
France
State/province [42] 0 0
Pessac
Country [43] 0 0
France
State/province [43] 0 0
Saint-Herblain
Country [44] 0 0
France
State/province [44] 0 0
Villejuif
Country [45] 0 0
Greece
State/province [45] 0 0
Athens
Country [46] 0 0
Greece
State/province [46] 0 0
Ioánnina
Country [47] 0 0
Korea, Republic of
State/province [47] 0 0
Gyeonggi-do
Country [48] 0 0
Korea, Republic of
State/province [48] 0 0
Incheon
Country [49] 0 0
Korea, Republic of
State/province [49] 0 0
Seoul
Country [50] 0 0
Korea, Republic of
State/province [50] 0 0
Suwon
Country [51] 0 0
Netherlands
State/province [51] 0 0
Amsterdam
Country [52] 0 0
Netherlands
State/province [52] 0 0
Den Haag
Country [53] 0 0
Norway
State/province [53] 0 0
Lørenskog
Country [54] 0 0
Norway
State/province [54] 0 0
Oslo
Country [55] 0 0
Philippines
State/province [55] 0 0
Cebu City
Country [56] 0 0
Philippines
State/province [56] 0 0
Ermita
Country [57] 0 0
Philippines
State/province [57] 0 0
Quezon City
Country [58] 0 0
Poland
State/province [58] 0 0
Poznan
Country [59] 0 0
Poland
State/province [59] 0 0
Warszawa
Country [60] 0 0
Romania
State/province [60] 0 0
Bucuresti
Country [61] 0 0
Romania
State/province [61] 0 0
Cluj-Napoca
Country [62] 0 0
Romania
State/province [62] 0 0
Craiova
Country [63] 0 0
Romania
State/province [63] 0 0
Timisoara
Country [64] 0 0
Russian Federation
State/province [64] 0 0
Arkhangel'sk
Country [65] 0 0
Russian Federation
State/province [65] 0 0
Barnaul
Country [66] 0 0
Russian Federation
State/province [66] 0 0
Chelyabinsk
Country [67] 0 0
Russian Federation
State/province [67] 0 0
Moscow
Country [68] 0 0
Russian Federation
State/province [68] 0 0
Omsk
Country [69] 0 0
Russian Federation
State/province [69] 0 0
Tomsk
Country [70] 0 0
Singapore
State/province [70] 0 0
Singapore
Country [71] 0 0
Spain
State/province [71] 0 0
Barcelona
Country [72] 0 0
Spain
State/province [72] 0 0
Madrid
Country [73] 0 0
Spain
State/province [73] 0 0
Valencia
Country [74] 0 0
Taiwan
State/province [74] 0 0
New Taipei City
Country [75] 0 0
Taiwan
State/province [75] 0 0
Taichung
Country [76] 0 0
Taiwan
State/province [76] 0 0
Tainan
Country [77] 0 0
Taiwan
State/province [77] 0 0
Taipei
Country [78] 0 0
Taiwan
State/province [78] 0 0
Taoyuan
Country [79] 0 0
Ukraine
State/province [79] 0 0
Dnipro
Country [80] 0 0
Ukraine
State/province [80] 0 0
Kharkiv
Country [81] 0 0
United Kingdom
State/province [81] 0 0
Dundee
Country [82] 0 0
United Kingdom
State/province [82] 0 0
London
Country [83] 0 0
United Kingdom
State/province [83] 0 0
Manchester

Funding & Sponsors
Primary sponsor type
Commercial sector/industry
Name
Debiopharm International SA
Address
Country
Other collaborator category [1] 0 0
Other
Name [1] 0 0
Caris Life Sciences
Address [1] 0 0
Country [1] 0 0
Other collaborator category [2] 0 0
Other
Name [2] 0 0
Optimal Research (Just In Time sites)
Address [2] 0 0
Country [2] 0 0

Ethics approval
Ethics application status

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for scientific queries

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
No/undecided IPD sharing reason/comment


What supporting documents are/will be available?




Results publications and other study-related documents

No documents have been uploaded by study researchers.


Results not provided in https://clinicaltrials.gov/study/NCT03834220