^
1d
Gentulizumab in Relapsed/Refractory Acute Myelogenous Leukemia or Myelodysplastic Syndrome (clinicaltrials.gov)
P1, N=58, Terminated, Changchun GeneScience Pharmaceutical Co., Ltd. | Recruiting --> Terminated; Adjusted the product development strategy.
Trial termination
1d
U96-CAR-T-Cells For R/R B-ALL (clinicaltrials.gov)
P1, N=30, Recruiting, The First Affiliated Hospital of Soochow University
New P1 trial
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CD20 negative
1d
Long-Term Follow-Up of Patients Who Have Participated in Children's Oncology Group Studies (clinicaltrials.gov)
P=N/A, N=5000, Active, not recruiting, Children's Oncology Group | Recruiting --> Active, not recruiting
Enrollment closed
1d
A Collaborative Palliative and Leukemia Care Model for Patients With AML and MDS Receiving Non-Intensive Therapy (clinicaltrials.gov)
P=N/A, N=320, Active, not recruiting, Massachusetts General Hospital | Trial completion date: Dec 2025 --> Dec 2026
Trial completion date
1d
Geriatric Optimization Plan to Improve Survival in Older Adult Allogeneic Hematopoietic Cell Transplant Candidates, OTIS Study (clinicaltrials.gov)
P=N/A, N=30, Completed, Ohio State University Comprehensive Cancer Center | Active, not recruiting --> Completed
Trial completion
1d
New P1 trial
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TP53 (Tumor protein P53)
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TP53 mutation • TP53 deletion
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Venclexta (venetoclax) • decitabine • Niktimvo (axatilimab-csfr)
1d
New P2 trial
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Venclexta (venetoclax) • cytarabine • azacitidine
1d
Trial initiation date
|
CD22 (CD22 Molecule)
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CD22 positive
1d
New P1 trial
|
Venclexta (venetoclax) • bortezomib • dexamethasone • Darzalex Faspro (daratumumab and hyaluronidase-fihj)
2d
Comparative evaluation of two NGS-based assays for somatic hypermutation analysis of IGHV genes in chronic lymphocytic leukemia. (PubMed, Blood Res)
These findings indicate that the Leader assay provides a more reliable assessment of SHM status, with higher concordance with SS. Although the FR1 assay may offer additional information regarding clonal patterns, its results should be interpreted cautiously. Given the limited sample size, further studies are warranted to validate these findings. Overall, the Leader assay appears to be more suitable as a primary tool for SHM evaluation, with FR1 results serving a complementary role when interpreted in clinical context.
Journal • Next-generation sequencing
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IGH (Immunoglobulin Heavy Locus)
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IGH mutation
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LymphoTrack® Dx IGH Assay