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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/ct2/show/NCT03905148




Registration number
NCT03905148
Ethics application status
Date submitted
3/04/2019
Date registered
5/04/2019
Date last updated
6/06/2023

Titles & IDs
Public title
Study of the Safety and Pharmacokinetics of BGB-283 (Lifirafenib) and PD-0325901 (Mirdametinib) in Participants With Advanced or Refractory Solid Tumors
Scientific title
A Phase 1b, Open-Label, Dose-escalation and Expansion Study to Investigate the Safety, Pharmacokinetics and Antitumor Activities of a RAF Dimer Inhibitor BGB-283 in Combination With MEK Inhibitor PD-0325901 in Patients With Advanced or Refractory Solid Tumors
Secondary ID [1] 0 0
BGB-283/PD-0325901-AU-001
Universal Trial Number (UTN)
Trial acronym
Linked study record

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

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

Experimental: Part A: Dose Escalation/Dose finding Dose Level Cohorts ranging in dose levels and dose regimens. - Combination doses of, Mirdametinib at once a day and lifirafenib at once a day And Mirdametinib at twice a day and lifirafenib at once a day

Experimental: Part B: Expansion - Approximately 20 participants with NRAS mutated solid tumors will be enrolled


Treatment: Drugs: Lifirafenib
RAF Dimer Inhibitor

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

Outcomes
Primary outcome [1] 0 0
Adverse Events and Serious Adverse Events
Timepoint [1] 0 0
Approximately 2 years from date of the participants enrollment
Primary outcome [2] 0 0
The incidence of DLT events and treatment-emergent AEs (TEAEs)
Timepoint [2] 0 0
Approximately 2 years from date of the participants enrollment
Primary outcome [3] 0 0
Objective response rate based on Response Evaluation Criteria in Solid Tumors (RECIST) Version 1.1 in participants with selected tumor types
Timepoint [3] 0 0
Approximately 2 years from date of the participants enrollment

Eligibility
Key inclusion criteria
Key

1. Able to provide informed consent

2. Age 18 on day of signing informed consent form (ICF) or of the legal age of consent in
the jurisdiction in which the study is taking place

3. Advanced or metastatic, unresectable tumors (other than patients with tumors of the
brain or central nervous system) who have experienced disease progression

- Part A: NSCLC, CRC, ovarian cancer, endometrial cancer, thyroid cancer, melanoma,
pancreatic cancer, and other)

- Part B: NRAS mutated solid tumors must have a known mutation status and a
histologically or cytologically confirmed advanced or refractory solid tumor. Up
to 40% Melanoma and Up to 20% CRC.

4. Must have archival tumor tissue or agree to tumor biopsy

5. Measurable disease per RECIST 1.1

6. Eastern Cooperative Oncology Group performance status of less than or equal to 1

7. Life expectancy is greater than 12 weeks of the signing of ICF.

8. Adequate organ function and no transfusion within 14 days of first dose.

9. Females are of non-child bearing potential or willing to use contraception.

10. Males vasectomized or agree to use contraception.

Key
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
1. Central Nervous System metastasis

2. Any retinal pathology considered to be a risk factor for central serous retinopathy

3. History of glaucoma

4. Active parathyroid disorder or history of malignancy associated hypercalcemia

5. Clinically significant cardiac disease within the past 6 months of signing ICF.

6. LVEF less than 50%

7. Abnormal QT interval at Screening

8. Severe uncontrolled systemic disease

9. HIV

10. Clinically significant active or known history of liver disease. (Hepatitis B and
Hepatitis C)

11. Hemorrhage or bleeding event at NCI-CTCAE v5.0 Grade 3 or higher within 28 days of
first dose.

12. history of or ongoing Von Willebrand disease and/or other past or present bleeding
disorders

13. Increased serum calcium

14. Inability to swallow oral medications

15. Ongoing radiation therapy or radio-cytotoxic therapy within prior 4 weeks. No
chemotherapy, immunotherapy, biologic therapy, hormonal, or molecular targeted therapy
within prior 2 weeks

16. Concomitant systemic or glucocorticoid therapy within 2 weeks

17. Major surgical procedure or significant traumatic injury within 4 weeks prior to first
dose or anticipates need for major surgery while on study

18. Concomitant medicines that are strong CYP3A inhibitors

19. History of toxicity from another RAF, MEK, ERK inhibitor requiring discontinuation of
treatment from these drugs

20. Underlying medical conditions in investigator's opinion to be unfavorable to be a part
of the study

21. Has been administered a live vaccine within 4 weeks (28 days) of initiation of study
treatment. NOTE: injectable seasonal vaccines for influenza and COVID-19 are generally
inactivated vaccines and are allowed. Intranasal vaccines are live vaccines and are
not allowed.

NOTE: Other protocol defined Inclusion/Exclusion criteria may apply.

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
Other
Other design features
Phase
Phase 1
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
1/05/2019
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
28/02/2026
Actual
Sample size
Target
105
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
NSW,VIC,WA
Recruitment hospital [1] 0 0
Blacktown Cancer and Haematology Centre - Blacktown
Recruitment hospital [2] 0 0
The Prince of Wales Private Hospital - Specialist Medical Randwick - Randwick
Recruitment hospital [3] 0 0
Peter MacCallum Cancer Centre - Melbourne
Recruitment hospital [4] 0 0
Linear Clinical Research - Nedlands
Recruitment postcode(s) [1] 0 0
2148 - Blacktown
Recruitment postcode(s) [2] 0 0
2031 - Randwick
Recruitment postcode(s) [3] 0 0
3000 - Melbourne
Recruitment postcode(s) [4] 0 0
6009 - Nedlands
Recruitment outside Australia
Country [1] 0 0
United States of America
State/province [1] 0 0
California
Country [2] 0 0
United States of America
State/province [2] 0 0
Texas

Funding & Sponsors
Primary sponsor type
Commercial sector/Industry
Name
BeiGene
Address
Country
Other collaborator category [1] 0 0
Commercial sector/Industry
Name [1] 0 0
SpringWorks Therapeutics, Inc.
Address [1] 0 0
Country [1] 0 0

Ethics approval
Ethics application status

Summary
Brief summary
This is a 2-part Phase 1b study of BGB-283 (lifirafenib) and PD-0325901 (mirdametinib)
combination in participants with tumors.
Trial website
https://clinicaltrials.gov/ct2/show/NCT03905148
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
BeiGene
Address 0 0
Country 0 0
Phone 0 0
1 (877) 828-5568
Fax 0 0
Email 0 0
[email protected]
Contact person for scientific queries



Summary Results

For IPD and results data, please see https://clinicaltrials.gov/ct2/show/NCT03905148