RecruitingPhase 1NCT07218913

Testing the Addition of Pedmark to Cisplatin Chemotherapy for Reducing Drug-Induced Ear Damage in Men With Stage II-III Metastatic Testicular Germ Cell Tumors

Phase 1 Trial of Pedmark in Men Receiving Cisplatin for Metastatic Germ Cell Tumor


Sponsor

City of Hope Medical Center

Enrollment

44 participants

Start Date

Feb 19, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

This phase I trial evaluates whether adding Pedmark to standard of care cisplatin-based chemotherapy reduces drug-induced ear damage (ototoxicity) in men with stage II-III testicular germ cell tumors that have spread from where they first started (primary site) to other places in the body (metastatic). Cisplatin is in a class of medications known as platinum-containing compounds. It works by killing, stopping or slowing the growth of tumor cells. Cisplatin-induced ototoxicity remains a major concern in adult patients with germ cell tumors as nearly four out of five patients develop hearing loss after treatment. Cisplatin is thought to cause ear damage by the production of chemically reactive molecules called reactive oxygen species. These molecules can cause damage when their levels get too high. Pedmark may reduce the negative side effects of cisplatin by neutralizing these reactive molecules. Pedmark has been approved for reducing the risk of cisplatin-induced ototoxicity in pediatric patients and older patients with solid tumors that haven't spread to other parts of the body. Adding Pedmark to cisplatin-based chemotherapy treatment may reduce ototoxicity in adult men with stage I-III testicular metastatic germ cell tumors.


Eligibility

Sex: MALEMin Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing whether adding a drug called Pedmark (sodium thiosulfate) to cisplatin chemotherapy can protect hearing in men with testicular cancer. Cisplatin is an effective chemotherapy, but it can cause permanent hearing loss. Pedmark is designed to reduce this side effect. **You may be eligible if...** - You are 18 or older and have confirmed testicular germ cell tumor (seminoma or non-seminoma) - Your cancer has spread (Stage II or III, metastatic) - You are currently receiving first or second-line cisplatin-based chemotherapy - Your planned total dose of cisplatin is 300 mg/m² or more - You are generally well enough for treatment (ECOG 0 or 1) - You are willing to have regular hearing tests (audiometry) **You may NOT be eligible if...** - You have had significant prior cancer treatment that has not resolved - Your blood counts (white blood cells, platelets, hemoglobin) are too low - Your kidney function is inadequate for cisplatin chemotherapy Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

PROCEDUREAudiometric Test

Ancillary studies

DRUGCisplatin

Given IV

PROCEDUREComputed Tomography

Undergo CT

PROCEDUREMagnetic Resonance Imaging

Undergo MRI

DRUGSodium Thiosulfate Anhydrous

Given IV


Locations(1)

City of Hope Medical Center

Duarte, California, United States

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NCT07218913


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