FS118 First in Human Study in Patients With Advanced Malignancies After PD-1/PD-L1 Containing Therapy
Status: | Recruiting |
---|---|
Conditions: | Cancer, Cancer, Cancer, Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 1/31/2019 |
Start Date: | April 16, 2018 |
End Date: | May 16, 2020 |
Contact: | Melinda Snyder |
Email: | FS118@f-star.com |
Phone: | 617-233-4057 |
A Phase 1, Open-Label, Dose-Escalation, and Cohort Expansion First-in-Human Study of the Safety, Tolerability, Pharmacokinetics, and Activity of FS118, a LAG-3/PD-L1 Bispecific Antibody, in Patients With Advanced Malignancies That Have Progressed On or After Prior PD-1/PD-L1 Containing Therapy
This study will be conducted in adult patients diagnosed with advanced tumors to characterize
the safety, tolerability, pharmacokinetics (PK), and activity of FS118. This is a Phase 1,
multi-center, open label, multiple-dose, first in human study, designed to systematically
assess safety and tolerability, and to identify the maximum tolerated dose (MTD) and/or
recommended Phase 2 dose (RP2D) for FS118 in patients with advanced tumors. Pharmacokinetics,
pharmacodynamics, immunogenicity, and response will also be assessed.
the safety, tolerability, pharmacokinetics (PK), and activity of FS118. This is a Phase 1,
multi-center, open label, multiple-dose, first in human study, designed to systematically
assess safety and tolerability, and to identify the maximum tolerated dose (MTD) and/or
recommended Phase 2 dose (RP2D) for FS118 in patients with advanced tumors. Pharmacokinetics,
pharmacodynamics, immunogenicity, and response will also be assessed.
Inclusion Criteria:
- Age ≥18 years;
- Patients with histologically confirmed, locally advanced, unresectable, or metastatic
solid tumors or hematological malignancies that progressed while on or after
PD-1/PD-L1 containing therapy;
- Measurable disease;
- Eastern Cooperative Oncology Group (ECOG) Performance Status ≤1;
- Life expectancy estimated to be at least 3 months;
- Highly effective contraception
- Willing and able to provide written informed consent.
Exclusion Criteria:
- Prior treatment with more than 1 checkpoint inhibitor (combination); prior treatment
with a lymphocyte-activation gene 3 (LAG-3) inhibitor; prior treatment with multi
specific checkpoint inhibitor molecules;
- Patients with active or documented history of autoimmune disease;
- History of uncontrolled intercurrent illness:
- Known infections:
- Uncontrolled CNS metastases, primary CNS tumors, or solid tumors with CNS metastases
as only measurable disease;
- Prior history of or active interstitial lung disease or pneumonitis, encephalitis,
seizures, severe immune related adverse events with prior PD-1/PD-L1 containing
treatments;
- Significant cardiac abnormalities;
- Significant laboratory abnormalities;
- Intolerance to the investigational product or its excipients, or any condition that
would significantly impair and/or prohibit the patient's participation in the study,
as per the Investigator's judgment.
We found this trial at
4
sites
Los Angeles, California 90095
Principal Investigator: Deborah Wong, MD, PhD
Phone: 310-794-6913
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Houston, Texas 77030
Principal Investigator: Timothy A Yap, MD, PhD
Phone: 713-745-6274
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333 Cedar St
New Haven, Connecticut 06504
New Haven, Connecticut 06504
(203) 432-4771
Principal Investigator: Patricia LoRusso, DO
Phone: 203-737-5228
Yale University School of Medicine Founded in 1810, the Yale School of Medicine is a...
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San Antonio, Texas 78229
Principal Investigator: Kyri Papadopoulos, MD
Phone: 210-593-5242
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