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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05228015
Other study ID # IK930-001
Secondary ID
Status Active, not recruiting
Phase Phase 1
First received
Last updated
Start date January 7, 2022
Est. completion date June 2025

Study information

Verified date June 2024
Source Ikena Oncology
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a Phase 1, first-in-human (FIH) clinical study to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and preliminary antitumor activity of IK-930, an oral TEAD inhibitor, administered orally (PO) as monotherapy in subjects with advanced solid tumors with or without gene alterations in the Hippo pathway for whom there are no further treatment options known to confer clinical benefit. The study consists of two phases, an initial Dose Escalation phase followed by a Dose Expansion phase.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 198
Est. completion date June 2025
Est. primary completion date June 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Signed informed consent must be obtained prior to participation in the study. 2. Male or female subjects = 18 years of age. 3. If feasible, subjects must be willing to consent to the submission of formalin-fixed paraffin-embedded tissue blocks or slides of tumor tissue, preferably from pre-treatment, baseline fresh tumor biopsy at Screening. Alternatively, archival tumor FFPE blocks or, unstained slides of tumor tissue from available archival sources are acceptable. 4. In the dose escalation cohort: Subjects with histologically proven advanced, unresectable, locally recurrent, or metastatic malignancy that has progressed on or following standard-of-care therapies and for whom there is no available therapy known to confer clinical benefit, regardless of the presence or absence of NF2 deficiency or other genetic alterations of the Hippo pathway. Subjects with histological confirmation of MPM; subjects with NF2-deficient MPM determined by local test results for testing can also be enrolled as well as subjects with any other solid tumors with documented NF2 deficiency determined by local test results for testing, including, but not limited to, meningioma, cholangiocarcinoma, thymoma, mucoepidermoid NSCLC, HCC, and others. Subjects diagnosed with EHE with documented TAZ-CAMTA1 or YAP1-TFE3 gene fusions, as determined by local tests and subjects with solid tumors who have YAP1/TAZ gene fusions as determined by local test results can also be enrolled in the dose escalation part of the study. 5. In the Dose expansion: Four groups of subjects will be enrolled: 1. Cohort 1: Subjects with histological confirmed MPM and that have documented NF2 deficiency, 2. Cohort 2: Subjects with other documented NF2-deficient solid tumors agnostic to tumor type including, but not limited to, meningioma, cholangiocarcinoma, thymoma, NSCLC, HCC, and others. 3. Cohort 3: Subjects with histopathological diagnosis of epithelioid hemangioendothelioma (EHE) and documented TAZ-CAMTA1 or YAP1-TFE3 gene fusions, as determined by local test results. Subjects who have objective disease progression to prior therapy or have active disease and cancer-related pain requiring narcotics for management are eligible. 4. Cohort 4: Subjects with any solid tumor with documented YAP1/TAZ gene fusions as determined by local test results. 6. In the Osimertinib Combination Cohort subjects must have a histologically proven, incurable, locally advanced or metastatic NSCLC expressing osimertinib-sensitive EGFR mutations; have evidence of radiological disease progression on prior receipt of Osimertinib and have progressed on additional anticancer therapy such as chemotherapy. 7. Subjects can have measurable or evaluable disease by RECIST 1.1 criteria as assessed by the Investigator/local radiologist. Exclusion Criteria: 1. Subjects with untreated or symptomatic primary central nervous system (CNS) tumors or with intracranial metastases (excluding primary CNS tumors that may be eligible for enrollment as part of Cohort 2 e.g., NF-2 deficient meningioma) a. Subjects with leptomeningeal metastases are excluded 2. Uncontrolled or life-threatening symptomatic concomitant disease 3. Clinically significant cardiovascular disease as defined in the protocol 4. Women who are pregnant or breastfeeding 5. Subjects who are unable to swallow or retain oral medication 6. Prior treatment/exposure to YAP/TAZ/TEAD inhibitors 7. Other inclusion/exclusion criteria may apply

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
IK-930
tablets for oral administration
Osimertinib
tablets for oral administration

Locations

Country Name City State
United Kingdom University Hospitals of Leicester NHS Trust Leicester England
United Kingdom The Royal Marsden Hospital London England
United States Massachusetts General Hospital Boston Massachusetts
United States The University of Chicago Chicago Illinois
United States Start Midwest Grand Rapids Michigan
United States MD Anderson Cancer Center Houston Texas
United States Sarah Cannon Research Institute Nashville Tennessee
United States Memorial Sloan Kettering Cancer Center New York New York
United States Sidney Kimmel Cancer Center at Thomas Jefferson University Hospital Philadelphia Pennsylvania
United States University of Pennsylvania Abramson Cancer Center Philadelphia Pennsylvania
United States Next Oncology San Antonio Texas

Sponsors (1)

Lead Sponsor Collaborator
Ikena Oncology

Countries where clinical trial is conducted

United States,  United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Safety and tolerability of IK-930 The frequency and severity, incidence of treatment-emergent and treatment-related adverse events using NCI-CTCAE v5.0 Through study completion, an average of 36 months
Primary Occurrence of Dose Limiting Toxicity during first treatment cycle Approximately 1 year
Primary RP2D and/or MTD of IK-930 Define the recommended phase 2 dose (RP2D) and/or MTD of IK-930 Approximately 1 year
Secondary Antitumor activity per RECIST 1.1: Disease control rate (DCR) of IK-930 as a single agent Through study completion, average of 36 months
Secondary Antitumor activity per RECIST 1.1: Time to response (TTR) of IK-930 as a single agent Through study completion, average of 36 months
Secondary Antitumor activity per RECIST 1.1: Duration of response (DOR) of IK-930 as a single agent Through study completion, average of 36 months
Secondary Antitumor activity per RECIST 1.1: Objective response rate (ORR) of IK-930 as a single agent Through study completion, average of 36 months
Secondary Antitumor activity: Median progression-free survival (PFS) of IK-930 as a single agent Through study completion, average of 36 months
Secondary Antitumor activity: Median overall survival (OS) of IK-930 as a single agent Through study completion, average of 36 months
Secondary Pharmacokinetics of IK-930: half-life (t1/2) Approximately 1 year
Secondary Pharmacokinetics of IK-930: Area Under the Curve (AUC) Approximately 1 year
Secondary Pharmacokinetics of IK-930: Maximum Plasma Concentration (Cmax) Approximately 1 year
Secondary Pharmacokinetics of IK-930: Minimum Plasma Concentration (Cmin) Approximately 1 year
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