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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT05566795




Registration number
NCT05566795
Ethics application status
Date submitted
16/09/2022
Date registered
4/10/2022
Date last updated
6/08/2024

Titles & IDs
Public title
DAY101 vs. Standard of Care Chemotherapy in Pediatric Patients With Low-Grade Glioma Requiring First-Line Systemic Therapy (LOGGIC/FIREFLY-2)
Scientific title
LOGGIC/FIREFLY-2: A Phase 3, Randomized, International Multicenter Trial of DAY101 Monotherapy Versus Standard of Care Chemotherapy in Patients With Pediatric Low-Grade Glioma Harboring an Activating RAF Alteration Requiring First-Line Systemic Therapy
Secondary ID [1] 0 0
DAY101-002
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Low-grade Glioma 0 0
Condition category
Condition code
Cancer 0 0 0 0
Brain

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Drugs - Tovorafenib
Treatment: Drugs - Chemotherapeutic Agent

Experimental: Arm #1 - Tovorafenib

Active comparator: Arm #2 - Investigator's choice of one of the following current standard of care for pediatric patients with low-grade gliomas:

1. Children's Oncology Group - Vincristine/Carboplatin (COG-V/C)
2. International Society for Paediatric Oncology - Low-Grade Glioma Vincristine/Carboplatin (SIOPe-LGG-V/C)
3. Vinblastine (VBL)


Treatment: Drugs: Tovorafenib
Oral type II RAF kinase inhibitor

Treatment: Drugs: Chemotherapeutic Agent
Intravenous solution for injection

Intervention code [1] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Compare the objective response rate (ORR) assessed per RANO-LGG criteria by Independent Review Committee (IRC) of tovorafenib monotherapy versus standard of care (SoC) chemotherapy
Timepoint [1] 0 0
Up to 60 months
Secondary outcome [1] 0 0
Compare the progression-free survival (PFS) assessed by IRC of tovorafenib monotherapy versus SoC chemotherapy per RANO-LGG criteria
Timepoint [1] 0 0
Up to 60 months
Secondary outcome [2] 0 0
Compare the duration of response (DOR) assessed by IRC of tovorafenib monotherapy versus SoC chemotherapy per RANO-LGG criteria
Timepoint [2] 0 0
Up to 60 months
Secondary outcome [3] 0 0
Compare the overall survival (OS) of tovorafenib monotherapy versus SoC chemotherapy
Timepoint [3] 0 0
Up to 60 months
Secondary outcome [4] 0 0
Compare the safety and tolerability of tovorafenib monotherapy versus SoC chemotherapy
Timepoint [4] 0 0
Up to 60 months
Secondary outcome [5] 0 0
Compare the safety and tolerability of tovorafenib monotherapy versus SoC chemotherapy
Timepoint [5] 0 0
Up to 60 months
Secondary outcome [6] 0 0
Evaluate changes in neurological function and adaptive behavior between tovorafenib versus SoC
Timepoint [6] 0 0
Up to 60 months
Secondary outcome [7] 0 0
Compare changes in visual function outcomes of tovorafenib monotherapy versus SoC chemotherapy in patients with optic pathway glioma (OPG)
Timepoint [7] 0 0
Up to 60 months
Secondary outcome [8] 0 0
Compare the ORR of tovorafenib monotherapy versus SoC chemotherapy as assessed by IRC per RANO-HGG and Response Assessment in Pediatric Neuro-Oncology (RAPNO-LGG) criteria
Timepoint [8] 0 0
Up to 60 months
Secondary outcome [9] 0 0
Compare the clinical bene?t rate (CBR) of tovorafenib monotherapy versus SoC chemotherapy as assessed by IRC per RANO-LGG, RANO-HGG and RAPNO-LGG criteria
Timepoint [9] 0 0
Up to 60 months
Secondary outcome [10] 0 0
Compare time to response (TTR) of tovorafenib monotherapy versus SoC chemotherapy as assessed by IRC per RANO-LGG, RANO-HGG and RAPNO-LGG criteria
Timepoint [10] 0 0
Up to 60 months
Secondary outcome [11] 0 0
Compare the PFS of tovorafenib monotherapy versus SoC chemotherapy as assessed by IRC per RAPNO-LGG and RANO-HGG criteria
Timepoint [11] 0 0
Up to 60 months
Secondary outcome [12] 0 0
Compare the DOR of tovorafenib monotherapy versus SoC chemotherapy as assessed by IRC per RAPNO-LGG and RANO-HGG criteria
Timepoint [12] 0 0
Up to 60 months
Secondary outcome [13] 0 0
Evaluate the health-related quality of life (HRQoL) in tovorafenib versus SoC chemotherapy using Patient-Reported Outcomes Measurement Information System (PROMIS) test battery
Timepoint [13] 0 0
Up to 60 months

Eligibility
Key inclusion criteria
* Less than 25 years of age with LGG with known activating RAF alteration
* Histopathologic diagnosis of glioma or glioneuronal tumor
* At least one measurable lesion as defined by RANO criteria
* Meet indication for first-line systemic therapy
Minimum age
No limit
Maximum age
25 Years
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
* Patient has any of the following tumor-histological findings:

1. Schwannoma
2. Subependymal giant cell astrocytoma (Tuberous Sclerosis)
3. Diffuse intrinsic pontine glioma, even if histologically diagnosed as World Health Organization (WHO) Grade I-II
* Patient's tumor has additional pathogenic molecular alterations, including but not limited to a) IDH 1/2 mutation, b) Histone H3 mutation, and c) NF-1 loss of function alteration.
* Known or suspected diagnosis of neurofibromatosis Type 1 or 2 (NF-1/NF-2)
* Prior or ongoing nonsurgical anticancer therapy for this indication (eg, chemotherapy, oral/intravenous targeted therapy) including radiation

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled 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 3
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Recruiting
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
Sample size
Target
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
QLD
Recruitment hospital [1] 0 0
Children's Health Queensland Hospital and Health Service - South Brisbane
Recruitment hospital [2] 0 0
Perth Children's Hospital - Nedlands
Recruitment hospital [3] 0 0
Women's and Children's Health Network - North Adelaide
Recruitment hospital [4] 0 0
The Royal Children's Hospital - Children's Cancer Centre - Parkville
Recruitment hospital [5] 0 0
Sydney Children's Hospital - Randwick - Randwick
Recruitment hospital [6] 0 0
Children's Hospital at Westmead - Westmead
Recruitment postcode(s) [1] 0 0
4101 - South Brisbane
Recruitment postcode(s) [2] 0 0
6009 - Nedlands
Recruitment postcode(s) [3] 0 0
5006 - North Adelaide
Recruitment postcode(s) [4] 0 0
3052 - Parkville
Recruitment postcode(s) [5] 0 0
2031 - Randwick
Recruitment postcode(s) [6] 0 0
2145 - Westmead
Recruitment outside Australia
Country [1] 0 0
United States of America
State/province [1] 0 0
Alabama
Country [2] 0 0
United States of America
State/province [2] 0 0
Arizona
Country [3] 0 0
United States of America
State/province [3] 0 0
California
Country [4] 0 0
United States of America
State/province [4] 0 0
Colorado
Country [5] 0 0
United States of America
State/province [5] 0 0
District of Columbia
Country [6] 0 0
United States of America
State/province [6] 0 0
Florida
Country [7] 0 0
United States of America
State/province [7] 0 0
Georgia
Country [8] 0 0
United States of America
State/province [8] 0 0
Illinois
Country [9] 0 0
United States of America
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Indiana
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United States of America
State/province [10] 0 0
Massachusetts
Country [11] 0 0
United States of America
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Michigan
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United States of America
State/province [12] 0 0
Missouri
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United States of America
State/province [13] 0 0
New York
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United States of America
State/province [14] 0 0
North Carolina
Country [15] 0 0
United States of America
State/province [15] 0 0
Ohio
Country [16] 0 0
United States of America
State/province [16] 0 0
Texas
Country [17] 0 0
United States of America
State/province [17] 0 0
Washington
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Austria
State/province [18] 0 0
Tirol
Country [19] 0 0
Austria
State/province [19] 0 0
Wien
Country [20] 0 0
Belgium
State/province [20] 0 0
Brussel
Country [21] 0 0
Belgium
State/province [21] 0 0
Ghent
Country [22] 0 0
Belgium
State/province [22] 0 0
Leuven
Country [23] 0 0
Canada
State/province [23] 0 0
Alberta
Country [24] 0 0
Canada
State/province [24] 0 0
British Columbia
Country [25] 0 0
Canada
State/province [25] 0 0
Quebec
Country [26] 0 0
Canada
State/province [26] 0 0
Québec
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Canada
State/province [27] 0 0
Toronto
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Czechia
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Brno
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Czechia
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Prague
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Denmark
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Midtjylland
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Denmark
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Copenhagen
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Finland
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Helsinki
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Finland
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Tampere
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France
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Lille
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France
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Lyon
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France
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Marseille
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France
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Paris
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France
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Villejuif
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Germany
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Baden-Württemberg
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Germany
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Bayern
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Germany
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Hessen
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Germany
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Sachsen
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Germany
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Berlin
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Germany
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Bielefeld
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Germany
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Hamburg
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Germany
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Heidelberg
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Germany
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Tübingen
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Germany
State/province [48] 0 0
Ulm
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Greece
State/province [49] 0 0
Athens
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Hungary
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Budapest
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Ireland
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Dublin
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Israel
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Petah tikva
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Israel
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Ramat Gan
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Italy
State/province [54] 0 0
Milan
Country [55] 0 0
Italy
State/province [55] 0 0
Rome
Country [56] 0 0
Italy
State/province [56] 0 0
Turin
Country [57] 0 0
Italy
State/province [57] 0 0
Bari
Country [58] 0 0
Italy
State/province [58] 0 0
Genova
Country [59] 0 0
Italy
State/province [59] 0 0
Napoli
Country [60] 0 0
Italy
State/province [60] 0 0
Padova
Country [61] 0 0
Italy
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Udine
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Korea, Republic of
State/province [62] 0 0
Seoul
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Netherlands
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Utrecht
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New Zealand
State/province [64] 0 0
Grafton
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Norway
State/province [65] 0 0
Troms
Country [66] 0 0
Norway
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Oslo
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Singapore
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Singapore
Country [68] 0 0
Slovenia
State/province [68] 0 0
Ljubljana
Country [69] 0 0
Spain
State/province [69] 0 0
Barakaldo
Country [70] 0 0
Spain
State/province [70] 0 0
Barcelona
Country [71] 0 0
Spain
State/province [71] 0 0
Madrid
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Spain
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Sevilla
Country [73] 0 0
Spain
State/province [73] 0 0
Valencia
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Sweden
State/province [74] 0 0
Göteborg
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Sweden
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Lund
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Sweden
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Stockholm
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Switzerland
State/province [77] 0 0
Lausanne
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Switzerland
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Zurich
Country [79] 0 0
United Kingdom
State/province [79] 0 0
England
Country [80] 0 0
United Kingdom
State/province [80] 0 0
Scotland
Country [81] 0 0
United Kingdom
State/province [81] 0 0
Surrey
Country [82] 0 0
United Kingdom
State/province [82] 0 0
Bristol
Country [83] 0 0
United Kingdom
State/province [83] 0 0
Cambridge

Funding & Sponsors
Primary sponsor type
Commercial sector/industry
Name
Day One Biopharmaceuticals, Inc.
Address
Country
Other collaborator category [1] 0 0
Other
Name [1] 0 0
SIOPe Brain Tumor Group LOGGIC Consortium
Address [1] 0 0
Country [1] 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
Day One Clinical Trials Information
Address 0 0
Country 0 0
Phone 0 0
650-484-0899
Fax 0 0
Email 0 0
Contact person for scientific queries

No information has been provided regarding IPD availability


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

No documents have been uploaded by study researchers.