Tovorafenib (DAY101) or in Combination With Pimasertib for Participants With Melanoma and Other Solid Tumors

Phase 1TerminatedNCT07121829

Day One Biopharmaceuticals, Inc.44 enrolled

Overview

This is a subprotocol of Master Protocol DAY101-102 and is a Phase 1b/2, multi-center, open label subprotocol of participants ≥12 years of age, with recurrent or progressive solid tumors with alterations in the key proteins of the MAPK pathway, such as tumors that harbor RAS or RAF alterations. \*Note: Study concluded as Phase 1b only.

Study Type

INTERVENTIONAL

Allocation

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Melanoma Solid Tumor Pilocytic Astrocytoma Non Small Cell Lung Cancer Colorectal Cancer Pancreatic Cancer

Interventions

TovorafenibDRUG

Tovorafenib tablet for oral use.

Tovorafenib Drug: PimasertibDRUG

Tovorafenib tablet for oral use. Pimasertib capsule for oral use

Eligibility

Sex: ALLMin age: 12 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Signed informed consent by participant ≥12 years of age; either a Consent or an Assent Form will be provided to the patient based on their capacity, local regulations, and guidelines. * Participants must have a report of histologically confirmed diagnosis of tumor and a concurrent MAPK pathway alteration (genomic alterations in RAS, RAF, MEK, or NF1) obtained through a tumor or liquid biopsy as assessed by genomic sequencing, polymerase chain reaction (PCR), fluorescence in situ hybridization (FISH), or another clinically accepted molecular diagnostic method recognized by local laboratory or regulatory agency * Participants must have radiographically stable, recurrent or progressive disease that is measurable using the appropriate tumor response criteria eg, (RECIST version 1.1, RANO) * Archival tumor tissue should be preferably less than 3 years old. If unavailable, a freshly acquired tumor tissue biopsy or liquid biopsy is required * If brain metastases are present, they must have been previously treated and be stable as assessed by radiographic imaging Exclusion Criteria: * Known presence of concurrent activating alterations * Participants with current evidence or a history of serous retinopathy (SR), retinal vein occlusion (RVO) or ophthalmopathy present at screening or baseline who would be considered at risk for SR or RVO * Participants who have an unstable neurological condition, despite adequate treatment (eg, uncontrolled seizures) * Participants with history of acute neurological events (such as intracranial or subarachnoid hemorrhage, stroke, intracranial trauma) within the past 6 months * History of second malignancy within 3 years prior to study treatment except for curatively treated cervical cancer in situ, non-melanoma skin cancer, or superficial bladder cancer

Locations (10)

The Angeles Clinic

Los Angeles, California, United States

Hoag Health

Newport Beach, California, United States

University of Colorado Hospital

Aurora, Colorado, United States

Cancer Specialists of North Florida

Jacksonville, Florida, United States

Community North Cancer Center

Indianapolis, Indiana, United States

OHSU Knight Cancer Institute

Portland, Oregon, United States

UPMC Hillman Cancer Center

Pittsburgh, Pennsylvania, United States

vanderbilt-Ingram Cancer Center

Nashville, Tennessee, United States

Princess Margaret Cancer Centre

Toronto, Ontario, Canada

The Hospital for Sick Children

Toronto, Ontario, Canada