A Phase 1, Open-label, Dose-finding and Cohort Expansion Study of ASN003 in Subjects With Advanced Solid Tumors

Status: Terminated
Location: See all (5) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 1
SUMMARY

The study is divided into two parts. The first part of the study will test various doses of ASN003 to find out the highest safe dose to test in three specific groups. The second part of the study will test how well ASN003 can control cancer. Subjects will be enrolled into one of three groups. Group 1: metastatic or recurrent melanoma with documented BRAFV600 mutation (n=20 evaluable patients) Group 2: metastatic colorectal cancer (CRC), or advanced non-small cell lung cancer (NSCLC) with documented BRAFV600 mutation (n=14 evaluable patients) Group 3: advanced solid tumors with documented PI3K pathway alterations (PIK3CA mutation or PTEN loss) (n=14 evaluable patients)

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• written informed consent obtained prior to any study-related procedures.

• Eastern Cooperative Oncology Group Performance Status: 0-1

• Part A only: Histologically or cytologically confirmed metastatic and/or advanced solid tumors with documented progressive disease for whom no further standard therapy is indicated.

• Part B only: 5. Histologically or cytologically confirmed, molecularly selected (i.e. BRAFV600 positive and/or PI3K mutation positive) advanced solid tumors. Prior molecular characterization should be based using a regulatory approved assay or analytically validated assay.

‣ Group 1: BRAFV600 positive metastatic or recurrent melanoma after failure of prior treatment with standard therapy such as a checkpoint inhibitor and an approved B-RAF inhibitor (vemurafenib or dabrafenib)

⁃ Group 2: BRAFV600 positive metastatic colorectal carcinoma (CRC), or advanced non-small cell lung carcinoma (NSCLC) after failure of at least two lines of prior standard therapy or for whom no further standard therapy is indicated.

⁃ Group 3: Advanced solid tumors with PI3K pathway alterations (PIK3CA mutation or PTEN loss) after failure of at least one line of prior standard therapy or for whom no further standard therapy is indicated. Prior treatment may not include inhibitors of the PI3K pathway.

• Screening hematology values of the following: absolute neutrophil count ≥ 1000/μL, platelets ≥ 100,000/μL, hemoglobin ≥ 10 g/dL (without transfusion support);

• Screening chemistry values of the following: alanine aminotransferase (ALT) and aspartate transaminase (AST) ≤ 3.0 × upper limit of the normal reference range (ULN), total bilirubin ≤ 2 × ULN, creatinine ≤ 1.5 × ULN, fasting blood glucose \< 140 mg/dL, hemoglobin A1C ≤ ULN, albumin ≥ 2.8 g/dL.

• Screening fasting lipid panel: LDL cholesterol \< 190 mg/dL, triglycerides \< 300 mg/dL

• Subject is willing and able to comply with all protocol required visits and assessments, including biopsy if assigned to the MTD expansion cohort;

Locations
United States
California
Cedars-Sinai Medical Center
Los Angeles
Florida
Moffitt Cancer Center
Tampa
Massachusetts
Massachusetts General Hospital
Boston
Michigan
START MidWest
Grand Rapids
Texas
South Texas Accelerated Research Therapeutics
San Antonio
Time Frame
Start Date: 2016-10
Completion Date: 2019-02
Participants
Target number of participants: 24
Treatments
Experimental: ASN003 Dose Escalation
Multiple ascending doses of ASN003 will be administered to determine the maximum tolerated dose (MTD).
Experimental: ASN003 MTD - BRAFv600 melanoma
ASN003 administered at the MTD in subjects with BRAF v600 mutated metastatic melanoma
Experimental: ASN003 MTD - BRAFv600 colon or lung cancer
ASN003 administered at the MTD in subjects with BRAFv600 mutated metastatic colorectal or non-small cell lung cancer.
Experimental: ASN003 MTD - PIK3 pathway mutated cancers
ASN003 administered at the MTD in subjects who have mutations in PI3 kinase or loss of PTEN.
Sponsors
Leads: Asana BioSciences

This content was sourced from clinicaltrials.gov

Similar Clinical Trials