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Résztvevőt keres itt: Egyesült Államok1. fázis

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

A legfontosabb adatok

Ki végzi
City of Hope Medical Center
Hol
Duarte (Egyesült Államok)A helyszín megnézése
Azonosító
Állapot
Toboroz
Fázis
1. fázis
Résztvevők
44 fő, tervezett
Kezdés
2026. febr. 19.
Várható befejezés
2031. jan. 22.
A vizsgálat típusa
Beavatkozással járó, 2 csoportAz egyik csoport egy már használt kezelést kap, összehasonlításként.
A vizsgált kezelések
  • Audiometric Test
  • Cisplatin
  • Computed Tomography
  • Magnetic Resonance Imaging
  • Sodium Thiosulfate Anhydrous
A regiszteradat frissítve
2026. április 17.

Ki vehet részt

MI-összefoglaló

A vizsgálat saját részvételi feltételeiből. Gép olvasta ki az oldalon álló regiszterszövegből, ezért tévedhet. Hogy ki vehet részt, azt a lenti regiszterszöveg és a vizsgálat csapata dönti el.

The trial is looking for adult men with testicular germ cell tumor that has spread (stage II or III). They must be getting cisplatin-based chemotherapy. The trial tests whether Pedmark protects hearing.

Életkor
18 years and older
Nem
Men only
A betegség stádiuma
Germ cell tumor (seminoma or non-seminoma) confirmed by tissue test, spread to other parts of the body (stage II or III). Disease must be measurable on scans (RECIST 1.1). ECOG 0 or 1 or Karnofsky score ≥ 70.
Korábbi kezelés
Must be receiving first or second line cisplatin-based chemotherapy, with a planned total cisplatin dose of ≥ 300mg/m^2 (including previous treatment). Must have recovered from side effects of earlier cancer treatment to grade 1 or less (hair loss allowed). No cisplatin-based therapy within 4 weeks before study treatment.

A részvétel fő kizáró okai

  • Moderate or worse hearing loss at the start
  • Brain metastases that cause symptoms, cancer in the brain lining, or past radiation to the head
  • Use of other drugs that can harm hearing, such as loop diuretics or aminoglycosides
  • Severe allergy to sodium thiosulfate, sulfites or thiols
  • Unable to have cisplatin due to heart, kidney or nerve problems or poor general health; or unstable heart disease

A regiszter feltételei, szó szerint

Mind a 32 feltétel megnézéseKevesebb

Ki vehet részt

  • Documented informed consent of the participant and/or legally authorized representative; Assent, when appropriate, will be obtained per institutional guidelines
  • Willing and able to sign informed consent form
  • Willing and able to participate in baseline and serial audiometry exams
  • Age: ≥ 18 years
  • Eastern Cooperative Oncology Group (ECOG) of 0 or 1 or Karnofsky score ≥ 70
  • Histologically confirmed germ cell tumor (seminoma or non-seminoma)
  • Presence of metastatic disease (stage II or III)
  • Fully recovered from the acute toxic effects (except alopecia) to ≤ grade 1 to prior anti-cancer therapy
  • Receiving first or second line cisplatin-based chemotherapy
  • Planned cumulative cisplatin dose of ≥ 300mg/m\^2 (including previous treatment)
  • Measurable disease per Response Evaluation Criteria in Solid Tumors (RECIST) 1.1
  • Absolute neutrophil count (ANC) ≥ 1,500/mm\^3
  • Platelets ≥ 100,000/mm\^3; NOTE: Platelet transfusions are not permitted within 14 days of platelet assessment unless cytopenia is secondary to disease involvement
  • Hemoglobin ≥ 9g/dL; NOTE: Red blood cell transfusions are not permitted within 14 days of hemoglobin assessment unless cytopenia is secondary to disease involvement
  • Total bilirubin ≤ 1.5 X upper limit of normal (ULN); Patients with known Gilbert disease who have serum bilirubin level < 3 x ULN may be enrolled
  • Aspartate aminotransferase (AST) ≤ 3.0 x ULN
  • Alanine aminotransferase (ALT) ≤ 3.0 x ULN
  • Creatinine clearance of ≥ 60 mL/min per the Cockcroft-Gault formula or serum creatinine ≤ 1.5 x ULN
  • * If not receiving anticoagulants: International normalized ratio (INR) OR prothrombin (PT) ≤ 1.5 x ULN; If on anticoagulant therapy: PT must be within therapeutic range of intended use of anticoagulants
  • * If not receiving anticoagulants: Activated partial thromboplastin time (aPTT) ≤ 1.5 x ULN; If on anticoagulant therapy: aPTT must be within therapeutic range of intended use of anticoagulants
  • Advise male patients with female partners of reproductive potential to use effective contraception during treatment and for 11 months after the last dose of cisplatin for injection

Ki nem vehet részt

  • Any cisplatin-based therapies within 4 weeks prior to initiation of study treatment
  • Chronic steroid use, defined as greater than prednisone 5 mg daily for longer than 21 days (steroids used as antiemetic during treatment is permitted)
  • Concurrent use of other ototoxic drugs other than cisplatin (loop diuretics, aminoglycosides, etc)
  • Known symptomatic brain metastases, leptomeningeal carcinomatosis, or prior cranial irradiation
  • Deemed cisplatin ineligible due to poor performance status, cardiac dysfunction, renal insufficiency, or significant peripheral neuropathy
  • Unstable cardiac disease as defined by one of the following:; Cardiac events such as myocardial infarction (MI) within the past 6 months; NYHA (New York Heart Association) heart failure class III-IV; Uncontrolled atrial fibrillation or hypertension
  • Patient must adhere to low sodium diet given other comorbidities
  • History of severe hypersensitivity to sodium thiosulfate or any components such as sulfites or thiols
  • If cisplatin infusion during study is planned to be longer than 6 hours, as Pedmark safety and efficacy has not been established when administered following longer cisplatin infusions
  • Greater than or equal to moderate hearing loss (HL) at baseline per World Health Organization (WHO) classification
  • Prospective participants who, in the opinion of the investigator, may not be able to comply with all study procedures (including compliance issues related to feasibility/logistics)

Helyszínek itt: Egyesült Államok

  • City of Hope Medical CenterDuarte, Egyesült ÁllamokContact: Alex Chehrazi-RaffleRésztvevőt keres

A vizsgálatról

Mit akar kideríteni a vizsgálat

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.

A vizsgálat 2 csoportja

  • Arm I (SOC cisplatin)Már használt kezelés, összehasonlításként

    Patients receive cisplatin IV over 60 minutes on days 1-5 or 2-5 of each SOC cisplatin-based chemotherapy regimen cycle. Cycles repeat every 21 days for 3-4 cycles in the absence of disease progression or unacceptable toxicity. Patients also undergo CT and/or MRI throughout the trial.

    Kezelés: Audiometric Test, Cisplatin, Computed Tomography és Magnetic Resonance Imaging

  • Arm II (SOC cisplatin, Pedmark)A vizsgált kezelés

    Patients receive cisplatin IV over 60 minutes on days 1-5 or 2-5 of each SOC cisplatin-based chemotherapy regimen cycle. Patients also receive Pedmark IV over 30 minutes, 6 hours after each SOC cisplatin infusion, on days 1-5 or 2-5 of each cycle. Cycles repeat every 21 days for 3-4 cycles in the absence of disease progression or unacceptable toxicity. Patients also undergo CT and/or MRI throughout the trial.

    Kezelés: Audiometric Test, Cisplatin, Computed Tomography, Magnetic Resonance Imaging és Sodium Thiosulfate Anhydrous

Kérdések a vizsgálat csapatának

  1. Milyen gyakran kell bejárnom, és egy-egy alkalom mennyi ideig tart?
  2. Megtérítik az utazási költséget?
  3. Megtarthatom a saját orvosomat?
  4. Mi történik, ha ki akarok lépni?

Contact the study team: see the registry record → Contacts and Locations

Oldal nyomtatása az orvosomnak

Adatok és források

Regiszteradat
Szerepel a ClinicalTrials.gov-on.
Hivatalos cím
Phase 1 Trial of Pedmark in Men Receiving Cisplatin for Metastatic Germ Cell Tumor
MI-összefoglaló
A vizsgálat saját részvételi feltételeiből. Gépi kiolvasás: 2026. november 14.
A regiszteradat frissítve
2026. április 17.