Anna Raciborska
Clinical trials sponsored by Anna Raciborska, explained in plain language.
Upcoming readouts
Trials from this sponsor expected to report results within the next 12 months.
- Can an antibody drug outsmart resistant Ewing's sarcoma? Results expected May 2027 (estimated)
- New hope for kids with rare blood disorder: trametinib trial launches Results expected Jun 2027 (estimated)
- New imaging test could spot rare childhood disease sooner Results expected Jun 2027 (estimated)
- New hope for kids with rare blood cancer: targeted drug trial launches Results expected Jun 2027 (estimated)
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Can an immune booster outsmart High-Risk bone cancer?
Disease control Recruiting nowThis trial is testing whether mifamurtide, a drug that stimulates the immune system to attack cancer cells, can improve outcomes for people with high-risk osteosarcoma, a type of bone cancer. Participants will be randomly assigned to receive either mifamurtide or the standard tre…
Phase 2 • Sponsor: Anna Raciborska • Aim: Disease control
Last updated Aug 28, 2026 00:00 UTC
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Can an antibody drug outsmart resistant Ewing's sarcoma?
Disease control Recruiting nowThis phase 2 trial is testing whether adding the antibody drug naxitamab to standard chemotherapy can help children and young adults with Ewing's sarcoma that has not responded to prior treatment. Participants must have a tumor that shows a specific marker called GD2. The study w…
Phase 2 • Sponsor: Anna Raciborska • Aim: Disease control
Last updated Aug 23, 2026 00:00 UTC
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New hope for kids with rare blood disorder: trametinib trial launches
Disease control Recruiting nowThis study tests the drug trametinib in children with histiocytosis, a rare blood disorder, that hasn't responded to standard treatments or has a specific genetic profile. The trial aims to find the best dose and timing to improve how long children live without their disease gett…
Phase 2 • Sponsor: Anna Raciborska • Aim: Disease control
Last updated Jun 27, 2026 12:01 UTC
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New hope for kids with rare blood cancer: targeted drug trial launches
Disease control Recruiting nowThis study tests the drug vemurafenib in children with a rare blood disorder called histiocytosis that has a specific gene mutation (BRAF) and hasn't improved with standard treatments. The goal is to find the best dose and how long to give the drug to stop the disease from gettin…
Phase 2 • Sponsor: Anna Raciborska • Aim: Disease control
Last updated Jun 27, 2026 12:00 UTC
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New imaging test could spot rare childhood disease sooner
Diagnosis Recruiting nowThis study aims to improve how doctors diagnose and monitor histiocytosis, a rare disease that causes abnormal cell growth, in children under 18. Researchers will use a special imaging agent called fluorodeoxyglucose (18F-FDG) in PET-CT scans, along with genetic testing of tumor …
Phase 3 • Sponsor: Anna Raciborska • Aim: Diagnosis
Last updated Aug 23, 2026 00:00 UTC