A Multi-Center, Open-Label, Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Anticancer Activity of Fruquintinib in Patients With Advanced Solid Tumors

Who is this study for? Adult patients with advanced solid tumors including breast cancer
What treatments are being studied? Fruquintinib
Status: Completed
Location: See all (9) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 1
SUMMARY

An open-label, dose escalation and expansion clinical trial to evaluate the safety, tolerability, and PK of fruquintinib in patients with advanced solid tumors, metastatic colorectal cancer and metastatic breast cancer.

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

• Fully understand the study and voluntarily sign the ICF;

• ≥18years of age;

• Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1;

⁃ Dose Escalation Phase:

⁃ • Histologically or cytologically documented, locally advanced or metastatic solid malignancy of any type (except squamous NSCLC) that has progressed on approved systemic therapy, and for whom no effective therapy or standard of care exists. This cohort is closed to enrollment.

⁃ Dose Expansion Phase:

• Cohort A: Histologically or cytologically documented, locally advanced or metastatic solid malignancy of any type (except squamous NSCLC), that has progressed on approved systemic therapy, and for whom no effective therapy or standard of care exists. This cohort is closed to enrollment.

• Cohort B: Histologically or cytologically documented mCRC in patients that have progressed on, or had intolerable toxicity with at least 1 FDA-approved third-line systemic therapy (trifluridine/tipiracil or regorafenib). Patients must also have been previously treated with fluoropyrimidine-, oxaliplatin-, and irinotecan-based chemotherapy, an anti-VEGF biological therapy, and an anti-EGFR therapy for patients who had RAS wild-type tumors. This cohort is currently enrolling.

• Cohort C: Histologically or cytologically documented adenocarcinoma of the colon or rectum. Patients must have progressed on, or had intolerable toxicity to, at least 2 prior regimens of standard chemotherapy, but must not have received prior TAS-102 or regorafenib. Prior therapy could have included adjuvant chemotherapy if a tumor had recurred within 6 months after the last administration of treatment. Patients must have been previously treated with fluoropyrimidine-, oxaliplatin-, and irinotecan-based chemotherapy, an anti-VEGF biological therapy and, if RAS wild-type, an anti-EGFR therapy

• Cohort D only: Histologically- or cytologically-confirmed Her2-negative, hormone receptor positive (ER+ and/or PR+) breast cancer

• Cohort E only: Histologically- or cytologically- confirmed triple negative breast cancer

Locations
United States
Arizona
Mayo Clinic Arizona
Phoenix
California
California Cancer Care Associates for Research & Excellence, Inc.
San Marcos
St. Joseph Heritage Healthcare
Santa Rosa
Colorado
University of Colorado Cancer Center
Aurora
Florida
Hem-Onc Associates of the Treasure Coast
Port Saint Lucie
Minnesota
Mayo Clinic Rochester
Rochester
Missouri
Washington University School of Medicine
Saint Louis
Tennessee
Vanderbilt Ingram Cancer Center
Nashville
Texas
MD Anderson Cancer Center
Houston
Time Frame
Start Date: 2017-12-11
Completion Date: 2023-03-30
Participants
Target number of participants: 129
Treatments
Experimental: 3 mg Dose Escalation
3 mg of Fruquintinib (HMPL-013), capsule taken orally, daily, 3 weeks on, 1 week off
Experimental: 5 mg Dose Escalation
5 mg of Fruquintinib (HMPL-013), capsule taken orally, daily, 3 weeks on, 1 week off
Experimental: Fruquintinib Expansion Cohort A
5 mg fruquintinib (HMPL-013) capsule taken orally, daily, 3 weeks on, 1 week off in patients with advanced solid tumors of any type.
Experimental: Metastatic Colorectal Cancer Expansion Cohort B (prior trifluridine/tipiracil or regorafenib)
5 mg fruquintinib (HMPL-013) capsule taken orally, daily, 3 weeks on, 1 week off in patients with metastatic colorectal cancer who have progressed on or had intolerable toxicity to TAS-102, regoragenib, or both.
Experimental: Metastatic Colorectal Cancer Expansion Cohort C (no prior trifluridine/tipiracil or regorafenib)
5 mg fruquintinib (HMPL-013) capsule taken orally, daily, 3 weeks on, 1 week off in patients with metastatic colorectal cancer who have not been treated with TAS-102 or regorafenib.
Experimental: Metastatic Breast Cancer (HR positive, HER2 negative) Expansion Cohort D
5 mg fruquintinib (HMPL-013) capsule taken orally, daily, 3 weeks on, 1 week off in patients with metastatic Her2-negative, hormone receptor positive breast cancer.
Experimental: Metastatic Breast Cancer (TNBC) Expansion Cohort E
5 mg fruquintinib (HMPL-013) capsule taken orally, daily, 3 weeks on, 1 week off in patients with metastatic triple negative (Her2-negative, ER-negative, PR-negative) breast cancer.
Related Therapeutic Areas
Sponsors
Leads: Hutchison Medipharma Limited

This content was sourced from clinicaltrials.gov

Similar Clinical Trials