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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/NCT04665206




Registration number
NCT04665206
Ethics application status
Date submitted
5/12/2020
Date registered
11/12/2020
Date last updated
13/05/2024

Titles & IDs
Public title
Study to Evaluate VT3989 in Patients With Metastatic Solid Tumors Enriched for Tumors With NF2 or mNF2 Gene Mutations
Scientific title
Phase 1, Multi-Center, Open-Label Study of VT3989 in Patients With Refractory Locally Advanced or Metastatic Solid Tumors Enriched for Tumors Harboring Mutations of the Neurofibromatosis Type 2 Gene (Mutant NF2 or mNF2)
Secondary ID [1] 0 0
VT3989-001
Universal Trial Number (UTN)
Trial acronym
Linked study record

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

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Drugs - VT3989

Experimental: VT3989 Dose Escalation - VT3989 dosed orally in 21 or 28 day cycles. Patients will be enrolled into escalating dose levels during the Dose Escalation Phase

Experimental: Dose Expansion - VT3989 dosed in 21 or 28 day cycles in patients with refractory metastatic solid tumors or mesothelioma, with or without NF2 mutant tumors.


Treatment: Drugs: VT3989
25, 50, 100,150 or 200 mg capsules for oral administration.
Intervention code [1] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Occurrence of Dose Limiting Toxicity
Timepoint [1] 0 0
over the first 21 days of dosing
Primary outcome [2] 0 0
Occurrence of General Toxicity
Timepoint [2] 0 0
through study completion, an average of 30 months
Secondary outcome [1] 0 0
Tumor Response
Timepoint [1] 0 0
through study completion, an average of 30 months
Secondary outcome [2] 0 0
Pharmacokinetic Evaluation - Cmax
Timepoint [2] 0 0
over first 21 days of dosing
Secondary outcome [3] 0 0
Pharmacokinetic Evaluation - Tmax
Timepoint [3] 0 0
over first 21 days of dosing
Secondary outcome [4] 0 0
Pharmacokinetic Evaluation - Half-life
Timepoint [4] 0 0
over first 21 days of dosing

Eligibility
Key inclusion criteria
- Part 1: pathologically diagnosed metastatic solid tumor or mesothelioma that has
progressed on or after all approved therapies of known clinical benefit except if the
patient refuses or is not a candidate for such therapy;

- Part 2: In mesothelioma cohorts, pathologically diagnosed advanced malignant
mesothelioma with or without NF2 mutations, that has progressed on or after all
approved therapies of known clinical benefit except if the patient refuses or is not a
candidate for such therapy. In the solid tumor cohort, pathologically diagnosed solid
tumor with with clearly inactivating NF2 mutations/alterations or YAP/TAZ gene
rearrangements, which have progressed on or after approved therapies of known clinical
benefit except if the patient refuses or is not a candidate for such therapy.

- Measurable disease per RECIST v1.1 for non-pleural mesothelioma or other solid tumors
(solid tumor expansion cohort) or modified RECIST v1.1 for malignant pleural
mesothelioma.

- ECOG: 0-1
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
- Active brain metastases or primary CNS (central nervous system) tumors.

- History of leptomeningeal metastases

- Active or chronic, uncontrolled bacterial, viral, or fungal infection(s) requiring
systemic therapy

- HIV positive or active Hepatitis B or Hepatitis C

- Clinically significant cardiovascular disease

- Additional active malignancy that may confound the assessment of the study endpoints

- Women who are pregnant or breastfeeding

- Prior treatment with TEAD inhibitor

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/Phase 2
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
24/03/2021
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
2/06/2027
Actual
Sample size
Target
250
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
VIC,WA
Recruitment hospital [1] 0 0
Monash Health - Clayton
Recruitment hospital [2] 0 0
Peter MacCullum Cancer Centre - Melbourne
Recruitment hospital [3] 0 0
Linear Clinical Research - Nedlands
Recruitment postcode(s) [1] 0 0
3168 - Clayton
Recruitment postcode(s) [2] 0 0
3000 - Melbourne
Recruitment postcode(s) [3] 0 0
6009 - Nedlands
Recruitment outside Australia
Country [1] 0 0
United States of America
State/province [1] 0 0
Illinois
Country [2] 0 0
United States of America
State/province [2] 0 0
Massachusetts
Country [3] 0 0
United States of America
State/province [3] 0 0
New York
Country [4] 0 0
United States of America
State/province [4] 0 0
Texas

Funding & Sponsors
Primary sponsor type
Commercial sector/Industry
Name
Vivace Therapeutics, Inc
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
This is an open-label, dose escalation and expansion study to evaluate the safety,
tolerability, PK, and biological activity of VT3989 administered once daily in 3- or 4-week
cycles in patients with mesothelioma and/or metastatic solid tumors that are resistant or
refractory to standard therapy or for which no effective standard therapy is available.
Trial website
https://clinicaltrials.gov/ct2/show/NCT04665206
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Neleesh Sharma, MD
Address 0 0
Vivace Therapeutics
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Heather Fritz
Address 0 0
Country 0 0
Phone 0 0
650-627-7437
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/NCT04665206