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Study identifier: NCT07728201 Synced from ClinicalTrials.gov · August 03, 2026
● Not Yet Recruiting

Response-adapted Luvometinib With or Without Cytarabine in Langerhans Cell Histiocytosis

Condition: Langerhans Cell Histiocytosis  ·  Sponsor: Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University

PhasePhase 2
Planned participants30
Who can joinAll sexes, 10 Years to no upper limit
Healthy volunteersNo

About this study

This single-center, prospective, interventional phase 2 study evaluates a response-adapted treatment strategy for patients aged 10 years and older with histologically confirmed Langerhans cell histiocytosis requiring systemic therapy. All participants receive six 35-day cycles of luvometinib induction. Post-induction treatment follows the cycle 6 PET/CT response: participants with complete metabolic response continue luvometinib maintenance without cytarabine, whereas participants without complete metabolic response who are judged suitable to continue protocol treatment receive luvometinib plus cytarabine followed by luvometinib maintenance; participants with progression or otherwise unsuitable to continue protocol treatment may receive other standard therapy or discontinue study treatment per protocol. The primary endpoint is objective response rate after six cycles by blinded independent central review.

This description comes directly from the study's public registry record.

Talk to the study team

Qi Zhu  ·  0086-18116215629  ·  zhuqi70@hotmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of MedicineShanghai, China

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