Recurrent Langerhans Cell Histiocytosis

2

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

Condition / disease
Location
Status: Recruiting

A Study With Tovorafenib (DAY101) as a Treatment Option for Progressive, Relapsed, or Refractory Langerhans Cell Histiocytosis

This phase II trial tests the safety, side effects, best dose and activity of tovorafenib (DAY101) in treating patients with Langerhans cell histiocytosis that is growing, spreading, or getting worse (progressive), has come back (relapsed) after previous treatment, or does not respond to therapy (refractory). Langerhans cell histiocytosis is a type of disease that occurs when the body makes too many immature Langerhans cells (a type of white blood cell). When these cells build up, they can form tumors in certain tissues and organs including bones, skin, lungs and pituitary gland and can damage them. This tumor is more common in children and young adults. DAY101 may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Using DAY101 may be effective in treating patients with relapsed or refractory Langerhans cell histiocytosis.

Participants needed: 48
Trial details
Phase: Phase 2Age: 180-22Biological sex: AllType: InterventionalSponsor: National Cancer Institute (NCI)Updated: Jun 17, 2026Locations: 118
Eligibility criteria

180 days- < 22 years (at time of study enrollment) [+48]

LCH arising along with other hematologic malignancy (e.g. mixed LCH with acute l... [+18]

Status: Recruiting

Q702 for the Treatment of Patients With Hematologic Malignancies

This phase I trial tests the safety, side effects, and best dose of Q702 in treating patients with hematologic malignancies. Q702 is in a class of medications called immunomodulatory agents. It works by helping the immune system kill cancer cells and by helping the bone marrow to produce normal blood cells. Giving Q702 may be safe, tolerable and/or effective in treating patients with hematologic malignancies.

Participants needed: 46
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: Mayo ClinicUpdated: Oct 10, 2025Locations: 2
Eligibility criteria

PRE-REGISTRATION: Age ≥ 18 years [+38]

PRE-REGISTRATION: Myeloproliferative neoplasm (MPN) patients with known active C... [+30]