Phase 2 Study of 9-ING-41 With Chemotherapy in Sarcoma

Withdrawn before enrolling · Phase 2

Conditions studied: Soft Tissue Sarcoma, Undifferentiated Pleomorphic Sarcoma, Myxofibrosarcoma, Leiomyosarcoma, Liposarcoma, Angiosarcoma, Synovial Sarcoma, Rhabdomyosarcoma, Spindle Cell Sarcoma, High Grade Sarcoma, Bone Sarcoma, Osteosarcoma, Ewing Sarcoma of Bone

In brief

This is an open label, two-stratum, phase 2 clinical trial evaluating the efficacy of 9-ING-41 in combination with gemcitabine/docetaxel in patients ≥10 years of age with advanced sarcoma. 9-ING-41 in combination with gemcitabine and docetaxel will lead to sustained disease control and/or increase the rates of objective response in patients with unresectable or metastatic soft tissue and bone sarcomas.

Key facts

Study ID

NCT05116800

Run by

Brown University

People needed

0

Starts

2022-03-01

Expected to finish

2030-08-01

Last updated by the study team

2021-12-07

Who can join

Age: 10 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Stratum A: Patients must have histologically confirmed grade 2 or 3 soft tissue sarcoma that is locally advanced and unresectable, or metastatic, consisting of one of the following subtypes: undifferentiated pleomorphic sarcoma (malignant fibrous histiocytoma), myxofibrosarcoma, leiomyosarcoma, liposarcoma (excluding well-differentiated), angiosarcoma, synovial sarcoma, rhabdomyosarcoma, spindle cell sarcoma and high-grade sarcoma NOS.
• Stratum B: Patients must have histologically confirmed bone sarcoma that is relapsed or refractory following front-line therapy consisting of one of the following subtypes: osteosarcoma and Ewing sarcoma.
• Patients must have at least one site of measurable disease by RECIST 1.1. See Section 12 (Measurement of Effect) for the evaluation of measurable disease.
• Stratum A: No more than three prior lines of systemic therapy. Of note, anthracycline-based chemotherapy is generally considered first-line therapy. Previously untreated patients may be enrolled at the discretion of the treating investigator.
• Stratum B: At least one prior line of systemic therapy.
• Age ≥10 years.
• Lansky score ≥50 for patients <16 years or ECOG performance status ≤2 for patients ≥16 years (Karnofsky ≥50%, see Appendix A).
• Life expectancy of greater than 12 weeks.
• Patients must have adequate organ and marrow function as defined below:
• Hemoglobin ≥8 g/dl
• absolute neutrophil count ≥1,000/mcL
• platelets ≥100,000/mcL (transfusion independent)
• total bilirubin ≤1.5x institutional upper limit of normal (ULN) (<3.0 mg/dL and direct bilirubin <1.5 mg/dL if documented Gilbert's syndrome)
• AST(SGOT)/ALT(SGPT) ≤2.5x institutional ULN (≤ 5 x ULN if liver metastases present)
• creatinine ≤1.5x institutional ULN OR
• glomerular filtration rate (GFR) ≥50 mL/min/1.73 m2
• PT/INR ≤1.5x institutional ULN
• Amylase and lipase ≤1.5x institutional ULN
• Washout period prior to Cycle 1, Day 1:
• ≥ 21 days since last dose of chemotherapy, immunotherapy, or therapeutic radiation treatment.
• ≥ 28 days since last tyrosine kinase inhibitor (or 5 half-lives, whichever is shorter).
• ≥ 7 days since last focal palliative radiation treatment.
• ≥ 28 days since major surgical procedure.
• Human immunodeficiency virus (HIV)-infected patients on effective anti-retroviral therapy with undetectable viral load within 6 months are eligible for this trial.
• For patients with evidence of chronic hepatitis B virus (HBV) infection, the HBV viral load must be undetectable on suppressive therapy, if indicated.

You may not qualify if…

• Patients with sarcoma histologies other than those listed above will be excluded.
• Prior treatment with 9-ING-41, gemcitabine, or docetaxel.
• Patients who have not recovered from adverse events due to prior anti-cancer therapy (i.e., have residual toxicities > Grade 1) with the exception of alopecia.
• Patients who are receiving any other investigational agents for treatment of their sarcoma.
• Patients who are pregnant or lactating.
• Patients with untreated brain or meningeal metastases. Subjects with history of metastases are eligible provided they do not require ongoing steroid treatment and have shown clinical and radiographic stability for at least 14 days after definitive therapy.
• History of allergic reactions attributed to compounds of similar chemical or biologic composition to 9-ING-41, gemcitabine, docetaxel, or other agents used in study.
• Patients with uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
• Has had a previous (within 2 years) or has a current malignancy other than the target cancer with the exception of curatively treated local tumors including carcinoma in situ of the breast or cervix, basal or squamous cell carcinoma of the skin, or prostate cancer with Gleason Grade < 6 and prostate-specific antigen within normal range.
• Has any medical and/or social condition that, in the opinion of the investigator would preclude study participation.

Where it is running

• Hasbro Children's Hospital — Providence, Rhode Island, United States
• Lifespan Cancer Insitute — Providence, Rhode Island, United States

Full record on ClinicalTrials.gov

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