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A Compassionate Use Program to Provide Access to Sodium Thiosulfate

A Compassionate Use Program to Provide Access to Sodium Thiosulfate for the Protection From Cisplatin-Induced Hearing Loss in Children Who Had Standard-risk Hepatoblastoma

Status
AVAILABLE
Phases
Unknown
Study type
Expanded Access
Source
ClinicalTrials.gov
Registry ID
NCT04132882
Enrollment
Unknown
Registered
2019-10-21
Start date
Unknown
Completion date
Unknown
Last updated
2021-09-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cisplatin-Induced Hearing Loss in Children Who Had Standard-risk Hepatoblastoma

Keywords

Cisplatin, Hearing Loss, Hepatoblastoma

Brief summary

This is a CUP which is designed to provide treatment access of STS to pediatric patients for the protection from Cisplatin-Induced Hearing Loss in children who had standard-risk hepatoblastoma. Approximately 10 patients will be treated as part of this program as specified below: Sodium Thiosulfate vials i.v. 80 mg/mL. This Compassionate Use Program for STS will consist of 2 phases: Screening: Patients will only be able to participate in this CUP if they meet the eligibility criteria. Treatment: Any clinical assessments, physical examinations, and dosage changes will be determined by the treating physician as per local standard medical practice. All serious adverse events (SAEs) will be reported. All related non-serious adverse events (AEs) will be reported where related means any event where a causal relationship between STS and the event is at least, a reasonable possibility. All non-serious AEs leading to dose modification or discontinuation will be reported. Pregnancies, outcomes of pregnancies, and exposure through breastfeeding will also be reported.

Interventions

DRUGSodium Thiosulfate (STS)

Sponsors

Fennec Pharma
CollaboratorUNKNOWN
TRPHARM
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
ALL
Age
1 Months to 18 Years

Inclusion criteria

I-1. Children older than 1 month and younger than 18 years of age who had standard-risk hepatoblastoma that had not been treated previously with STS and receive cisplatin. I-2. A written informed consent was provided from all the patients and/or parents or legal guardians of children.

Exclusion criteria

E-1. Any previous participation in an STS clinical trial. E-2. Participation in another clinical study with an investigational product during the most recent chemotherapy course. E-3. Patients with a known hypersensitivity to STS or any of the excipients of the product. E-4. Patients receiving any systemic chemotherapy or radiotherapy (except for palliative reasons) or major surgery within 3 weeks prior to STS treatment. E-5. Persistent toxicities (\>Common Terminology Criteria for Adverse Event (CTCAE) CTCAE grade 2) caused by previous cancer therapy, excluding alopecia. E-6. Breast feeding or pregnant women.

Countries

Turkey (Türkiye)

Contacts

Primary ContactSerdar Altinel
serdar.altinel@trpharm.com00902123863149

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026