Hepatotoxicity

3

Review clinical trials related to Hepatotoxicity. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

A Long-term Study Evaluating Hepatotoxicity Associated With TURALIO™ (Pexidartinib) Treatment

A study to evaluate the long-term risk of hepatic failure with TURALIO™ (pexidartinib) and the mechanism of liver injury based upon optional liver biopsy information among patients who received or are receiving TURALIO™ (pexidartinib) and experience hepatotoxicity.

Participants needed: 30
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Daiichi SankyoUpdated: Oct 6, 2025Locations: 8Duration: 10 Years
Eligibility criteria

Adult participants with symptomatic TGCT associated with severe morbidity or fun... [+6]

Not applicable

Status: Recruiting

Use of Levocarnitine to Reduce Asparaginase Hepatotoxicity in Patients With Acute Lymphoblastic Leukemia

Acute lymphoblastic leukemia (ALL) is the most common cancer seen in pediatric oncology. The necessary chemotherapy for pediatric and adolescent and young adult (AYA) patients with ALL includes steroids, anthracyclines, asparaginase, and vincristine. One of the most hepatotoxic chemotherapy agents is asparaginase, with treatment-associated hepatotoxicity (TAH) observed in up to 60% of patients. The frequency of TAH is increased in overweight or obese patients of Latino heritage. Carnitine is a naturally-derived compound that is produced in the liver and kidneys; it is found in certain foods, such as meat, poultry, fish, and some dairy products. Endogenous carnitine transports long-chain fatty acids into the mitochondria, where they are oxidized to produce energy, and acts as scavengers of oxygen free radicals. Thus, carnitine can reduce oxidative stress and modulate inflammatory response. Levocarnitine is a supplement form of carnitine used typically in the care and management of patients with carnitine deficiency. Pediatric and AYAs with ALL will be given oral levocarnitine as a supplement during their initial phases of treatment, when the most hepatotoxic agents are administered, to determine if the incidence of liver toxicity can be reduced or eliminated.

Participants needed: 20
Trial details
Phase: Early Phase 1Age: 5-29Biological sex: AllType: InterventionalSponsor: Children's Hospital of Orange CountyUpdated: Aug 21, 2024Locations: 2
Eligibility criteria

Patients aged 5 to < 30 years [+3]

Known allergic reaction to levocarnitine or its components [+5]

Status: Not yet recruiting

Proof-of-concept to Evaluate the Efficacy and Safety of Prednisone in Idiosyncratic Hepatotoxicity

This trial´s aim is to assess if oral prednisone (compared to placebo), administered over five weeks is beneficial in terms of decreased total bilirubin (TBL): reduction of the peak of TBL at least 50% at 14 days or reduction in the time to normalisation of TBL value.

Participants needed: 60
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Fundación Pública Andaluza para la Investigación de Málaga en Biomedicina y SaludUpdated: Apr 5, 2024
Eligibility criteria

Female and male patients, aged ≥ 18 years. [+3]

No clear DILI diagnosis after an expert committee DILI assessment. [+10]