T-cell prolymphocytic leukemia
diseaseOn this page
Also known as chronic T-cell leukaemiachronic T-cell leukemiachronic T-cell lymphocytic leukaemiachronic T-cell lymphocytic leukemiaCLL, T-cellleukemia, T-cell, chronicT cell chronic lymphocytic leukaemiaT cell chronic lymphocytic leukemiaT cell CLLT cell prolymphocytic leukaemiaT cell prolymphocytic leukemiaT prolymphocytic leukaemiaT prolymphocytic leukemiaT-cell chronic lymphocytic leukaemiaT-cell chronic lymphocytic leukemiaT-cell CLLT-PLLTPLL
Summary
T-cell prolymphocytic leukemia (MONDO:0019468) is a cancer with 1 cohort gene (1 CIViC-evidence somatic driver; 4 ClinVar predisposition records) and 26 clinical trials. Top therapeutic interventions include fludarabine phosphate, duvelisib, and carmustine.
At a glance
- Classification: Cancer
- Prevalence: Unknown (Worldwide) [Orphanet-validated]
- Cohort genes: 1
- ClinVar variants: 4
- Clinical trials: 26
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | T-cell prolymphocytic leukemia |
| Mondo ID | MONDO:0019468 |
| EFO | EFO:1000560 |
| MeSH | D015461 |
| Orphanet | 86871 |
| DOID | DOID:0081042 |
| ICD-11 | 352523899 |
| NCIT | C4752 |
| SNOMED CT | 277545003, 277567002 |
| UMLS | C2363142 |
| MedGen | 391707 |
| GARD | 0013731 |
| MedDRA | 10042985 |
| Is cancer (heuristic) | yes |
Also known as: chronic T-cell leukaemia · chronic T-cell leukemia · chronic T-cell lymphocytic leukaemia · chronic T-cell lymphocytic leukemia · CLL, T-cell · leukemia, T-cell, chronic · T cell chronic lymphocytic leukaemia · T cell chronic lymphocytic leukemia · T cell CLL · T cell prolymphocytic leukaemia · T cell prolymphocytic leukemia · T prolymphocytic leukaemia · T prolymphocytic leukemia · T-cell chronic lymphocytic leukaemia · T-cell chronic lymphocytic leukemia · T-cell CLL · T-cell prolymphocytic leukemia · T-PLL · TPLL
Data availability: 4 ClinVar variants · 4 cell lines.
Disease family
Classification path: disease by etiologic mechanism › cancer or benign tumor › neoplastic disease or syndrome › neoplasm › hematopoietic and lymphoid system neoplasm › hematopoietic and lymphoid cell neoplasm › lymphoid neoplasm › T-cell and NK-cell neoplasm › neoplasm of mature T-cells or NK-cells › mature T-cell and NK-cell non-Hodgkin lymphoma › T-cell prolymphocytic leukemia
Related subtypes (7): angioimmunoblastic T-cell lymphoma, systemic Epstein-Barr virus-positive T-cell lymphoproliferative disease of childhood, hydroa vacciniforme-like lymphoma, T-cell large granular lymphocyte leukemia, aggressive NK-cell leukemia, anaplastic large cell lymphoma, breast implant-associated anaplastic large cell lymphoma
Genetics & variants
GWAS landscape
No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.
Variant details and genetic-evidence tiers
ClinVar germline variants
4 retrieved; paginated sample, class counts are floors:
2 pathogenic, 1 pathogenic/likely pathogenic, 1 uncertain significance
| ClinVar | Variant (HGVS) | Gene | Classification | Review |
|---|---|---|---|---|
| 3019 | NM_000051.4(ATM):c.7638_7646del (p.Arg2547_Ser2549del) | ATM | Pathogenic/Likely pathogenic | criteria provided, multiple submitters, no conflicts |
| 3023 | NM_000051.4(ATM):c.7271T>G (p.Val2424Gly) | ATM | Pathogenic | reviewed by expert panel |
| 3042 | NM_000051.4(ATM):c.5309C>G (p.Ser1770Ter) | ATM | Pathogenic | criteria provided, multiple submitters, no conflicts |
| 3026 | NM_000051.4(ATM):c.5044G>C (p.Asp1682His) | ATM | Uncertain significance | criteria provided, single submitter |
Genes & proteins
Mendelian disease overlap and somatic drivers
GenCC: 0 · Orphanet: 8 · OMIM-shared: 0 · Dual-evidence (GWAS+Mendelian): 0
Somatic driver evidence (intOGen + CIViC, cohort fanout)
| Gene | intOGen role | Cancer types | CIViC |
|---|---|---|---|
| ATM | LoF | BLCA,BRCA,CCRCC,CHOL,CLLSLL,COAD,COADREAD,ESCA,HCC,LUAD,LUSC,MEL,NSCLC,PAAD,PANCREAS,PANET,PCM,PLMESO,PRAD,PROSTATE,STAD,UCEC,UTUC,WDTC | CIViC #69 |
Orphanet rare-disease linkage (cohort genes)
| Gene | Orphanet ID | Rare disease |
|---|---|---|
| ATM | Orphanet:100 | Ataxia-telangiectasia |
| ATM | Orphanet:1331 | Familial prostate cancer |
| ATM | Orphanet:145 | Hereditary breast and/or ovarian cancer syndrome |
| ATM | Orphanet:227535 | Hereditary breast cancer |
| ATM | Orphanet:370109 | Ataxia-telangiectasia variant |
| ATM | Orphanet:440437 | Familial colorectal cancer Type X |
| ATM | Orphanet:52416 | Mantle cell lymphoma |
| ATM | Orphanet:67038 | B-cell chronic lymphocytic leukemia |
Cohort genes → proteins
1 cohort genes, 1 distinct canonical proteins.
Evidence partition
| Subset | Genes |
|---|---|
| multi_evidence | 1 |
Cohort genes (full)
| Symbol | HGNC | Ensembl | UniProt | Name | Evidence |
|---|---|---|---|---|---|
| ATM | HGNC:795 | ENSG00000149311 | Q13315 | Serine-protein kinase ATM | clinvar |
Cohort function summary
Lead sentence per gene, UniProt-curated.
| Symbol | Protein name | Function (lead sentence) |
|---|---|---|
| ATM | Serine-protein kinase ATM | Serine/threonine protein kinase which activates checkpoint signaling upon double strand breaks (DSBs), apoptosis and genotoxic stresses such as ionizing ultraviolet A light (UVA), thereby acting as a DNA damage sensor. |
Protein-family classification
Druggable: 1 · Difficult: 0 · Unknown: 0 · Druggable fraction: 1.0
Family distribution
Cohort families vs a genome-wide background (hypergeometric, BH-FDR; fold = observed/expected). Counts kept; sorted by enrichment, so the catch-all Other/Unknown bucket no longer leads.
| Family | Genes | Fold | FDR |
|---|---|---|---|
| Kinase | 1 | 27.7× | 0.036 |
Per-gene assignment
| Symbol | Family | Druggable? | EC | InterPro (top 3) |
|---|---|---|---|---|
| ATM | Kinase | yes | 2.7.11.1 | PI3/4_kinase_cat_dom, PIK-rel_kinase_FAT, FATC_dom |
Expression context
Cohort genes with no expression data: 0.
1 cohort gene are a single-cell marker in ≥1 SCXA experiment.
Breadth distribution (Bgee present_calls)
| Bucket | Genes |
|---|---|
| narrow (1-5 tissues) | 0 |
| moderate (6-20) | 0 |
| broad (>20) | 1 |
| unknown | 0 |
Top tissues across cohort
| Tissue | Cohort genes |
|---|---|
| calcaneal tendon | 1 |
| colonic epithelium | 1 |
| corpus callosum | 1 |
Per-gene tissue summary (top 30)
| Symbol | Bgee breadth | FANTOM5 breadth | SCXA | Top tissues |
|---|---|---|---|---|
| ATM | 286 | ubiquitous | marker | calcaneal tendon, colonic epithelium, corpus callosum |
Protein interactions among cohort
Intra-cohort edges: 0.
Hub genes (top 10 by interactor count)
| Symbol | Interactor count |
|---|---|
| ATM | 7,383 |
Structural data
PDB: 1 · AlphaFold-only: 0 · No structure: 0
Cohort genes with PDB structures (top 30)
| Symbol | UniProt | PDB entries |
|---|---|---|
| ATM | Q13315 | 14 |
Function
Pathway analysis
Distinct Reactome pathways touched by cohort: 61. Enrichment computed across 1 evidence-associated genes (1 with Reactome annotation).
Pathways by enrichment
Over-representation of cohort genes vs the genome-wide background (hypergeometric test, Benjamini-Hochberg FDR; fold = observed/expected over 1 annotated cohort genes). Counts and members are kept as ground-truth; sorted by enrichment.
| Pathway | Cohort genes | Fold | FDR | Sample cohort genes |
|---|---|---|---|---|
| Sensing of DNA Double Strand Breaks | 1 | 1903.3× | 0.007 | ATM |
| TP53 Regulates Transcription of Caspase Activators and Caspases | 1 | 951.7× | 0.007 | ATM |
| Pexophagy | 1 | 951.7× | 0.007 | ATM |
| Defective homologous recombination repair (HRR) due to PALB2 loss of function | 1 | 951.7× | 0.007 | ATM |
| Diseases of DNA Double-Strand Break Repair | 1 | 815.7× | 0.007 | ATM |
| Defective homologous recombination repair (HRR) due to BRCA2 loss of function | 1 | 815.7× | 0.007 | ATM |
| Stabilization of p53 | 1 | 761.3× | 0.007 | ATM |
| p53-Dependent G1 DNA Damage Response | 1 | 713.8× | 0.007 | ATM |
| p53-Dependent G1/S DNA damage checkpoint | 1 | 713.8× | 0.007 | ATM |
| G1/S DNA Damage Checkpoints | 1 | 671.8× | 0.007 | ATM |
| Resolution of D-Loop Structures | 1 | 634.4× | 0.007 | ATM |
| Diseases of DNA repair | 1 | 571.0× | 0.007 | ATM |
| TP53 Regulates Transcription of Cell Death Genes | 1 | 543.8× | 0.007 | ATM |
| TP53 Regulates Transcription of Genes Involved in Cytochrome C Release | 1 | 543.8× | 0.007 | ATM |
| Regulation of TP53 Activity through Methylation | 1 | 543.8× | 0.007 | ATM |
| Regulation of TP53 Expression and Degradation | 1 | 519.1× | 0.007 | ATM |
| DNA Double Strand Break Response | 1 | 475.8× | 0.007 | ATM |
| Impaired BRCA2 binding to PALB2 | 1 | 456.8× | 0.007 | ATM |
| Defective homologous recombination repair (HRR) due to BRCA1 loss of function | 1 | 423.0× | 0.007 | ATM |
| Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA1 binding function | 1 | 423.0× | 0.007 | ATM |
| Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA2/RAD51/RAD51C binding function | 1 | 423.0× | 0.007 | ATM |
| Cellular response to heat stress | 1 | 393.8× | 0.007 | ATM |
| Resolution of D-loop Structures through Synthesis-Dependent Strand Annealing (SDSA) | 1 | 393.8× | 0.007 | ATM |
| Homologous DNA Pairing and Strand Exchange | 1 | 380.7× | 0.007 | ATM |
| Homology Directed Repair | 1 | 308.6× | 0.007 | ATM |
| HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | 1 | 308.6× | 0.007 | ATM |
| Impaired BRCA2 binding to RAD51 | 1 | 308.6× | 0.007 | ATM |
| Resolution of D-loop Structures through Holliday Junction Intermediates | 1 | 300.5× | 0.007 | ATM |
| HDR through Single Strand Annealing (SSA) | 1 | 292.8× | 0.007 | ATM |
| Regulation of TP53 Degradation | 1 | 292.8× | 0.007 | ATM |
GO biological processes by enrichment
Over-representation of cohort genes vs the genome-wide background (hypergeometric test, Benjamini-Hochberg FDR; fold = observed/expected over 1 annotated cohort genes). Counts and members are kept as ground-truth; sorted by enrichment.
| GO term | Cohort genes | Fold | FDR | Sample cohort genes |
|---|---|---|---|---|
| establishment of RNA localization to telomere | 1 | 8426.0× | 0.002 | ATM |
| establishment of protein-containing complex localization to telomere | 1 | 8426.0× | 0.002 | ATM |
| positive regulation of telomerase catalytic core complex assembly | 1 | 8426.0× | 0.002 | ATM |
| pre-B cell allelic exclusion | 1 | 5617.3× | 0.002 | ATM |
| cellular response to nitrosative stress | 1 | 5617.3× | 0.002 | ATM |
| peptidyl-serine autophosphorylation | 1 | 3370.4× | 0.003 | ATM |
| negative regulation of telomere capping | 1 | 3370.4× | 0.003 | ATM |
| regulation of telomere maintenance via telomerase | 1 | 2808.7× | 0.003 | ATM |
| positive regulation of telomere maintenance via telomere lengthening | 1 | 2808.7× | 0.003 | ATM |
| lipoprotein catabolic process | 1 | 2407.4× | 0.003 | ATM |
| V(D)J recombination | 1 | 2106.5× | 0.003 | ATM |
| meiotic telomere clustering | 1 | 1872.4× | 0.003 | ATM |
| female meiotic nuclear division | 1 | 1685.2× | 0.003 | ATM |
| histone mRNA catabolic process | 1 | 1685.2× | 0.003 | ATM |
| cellular response to X-ray | 1 | 1685.2× | 0.003 | ATM |
| DNA double-strand break processing | 1 | 1532.0× | 0.003 | ATM |
| regulation of autophagosome assembly | 1 | 1123.5× | 0.003 | ATM |
| pexophagy | 1 | 1053.2× | 0.003 | ATM |
| regulation of cellular response to heat | 1 | 1053.2× | 0.003 | ATM |
| positive regulation of DNA damage response, signal transduction by p53 class mediator | 1 | 991.3× | 0.003 | ATM |
| replicative senescence | 1 | 991.3× | 0.003 | ATM |
| negative regulation of B cell proliferation | 1 | 936.2× | 0.003 | ATM |
| oocyte development | 1 | 936.2× | 0.003 | ATM |
| cellular response to stress | 1 | 842.6× | 0.003 | ATM |
| signal transduction in response to DNA damage | 1 | 802.5× | 0.003 | ATM |
| positive regulation of telomere maintenance via telomerase | 1 | 732.7× | 0.004 | ATM |
| cellular response to gamma radiation | 1 | 601.9× | 0.004 | ATM |
| mitotic spindle assembly checkpoint signaling | 1 | 561.7× | 0.004 | ATM |
| reciprocal meiotic recombination | 1 | 561.7× | 0.004 | ATM |
| male meiotic nuclear division | 1 | 543.6× | 0.004 | ATM |
Therapeutics
Drugs indicated for this disease
No approved or late-stage (phase ≥3) drug is indicated for this disease; the following are in earlier-phase trials only.
Earlier-phase candidates (phase 2, investigational — efficacy not yet established): Cyclosporine, Fludarabine Phosphate, Ibrutinib, Mycophenolate Mofetil, Venetoclax.
Drug target analysis
Approved (phase 4): 1 · Phase ≥3: 1 · Phased (≥1): 1 · Undrugged: 0
Druggability breadth: 1 of 1 evidence-associated genes (100%) have a ChEMBL target (buckets above are over the deeply-mined display cohort).
Genes with an approved drug
The molecule shown is one approved compound that hits the gene — not necessarily a drug of choice or one indicated for this disease.
| Symbol | Example approved molecule |
|---|---|
| ATM | AMIODARONE HYDROCHLORIDE |
Top cohort targets by molecule count
| Symbol | Molecules | Max phase |
|---|---|---|
| ATM | 35 | 4 |
Drugs targeting cohort genes (top 30)
| Molecule | Max phase | Targets in cohort |
|---|---|---|
| AMIODARONE HYDROCHLORIDE | 4 | ATM |
| FURAZOLIDONE | 4 | ATM |
| ESTRADIOL ACETATE | 4 | ATM |
| NAFTIFINE HYDROCHLORIDE | 4 | ATM |
| METHYSERGIDE MALEATE | 4 | ATM |
| AMITRIPTYLINE HYDROCHLORIDE | 4 | ATM |
| XYLOMETAZOLINE HYDROCHLORIDE | 4 | ATM |
| FLUVOXAMINE MALEATE | 4 | ATM |
| ESTRADIOL VALERATE | 4 | ATM |
| PERMETHRIN | 4 | ATM |
| MITOTANE | 4 | ATM |
| TICLOPIDINE HYDROCHLORIDE | 4 | ATM |
| ENOXIMONE | 4 | ATM |
| METHYLENE BLUE ANHYDROUS | 4 | ATM |
| DITHIAZANINE IODIDE | 4 | ATM |
| ETHACRYNIC ACID | 4 | ATM |
| SECNIDAZOLE | 4 | ATM |
| MENADIONE | 4 | ATM |
| FENOFIBRATE | 4 | ATM |
| DIPYRIDAMOLE | 4 | ATM |
| DACTOLISIB | 3 | ATM |
| STREPTONIGRIN | 2 | ATM |
| CALCIMYCIN | 2 | ATM |
| ENPIROLINE | 2 | ATM |
| OXACEPROL | 2 | ATM |
| TOLONIUM CHLORIDE | 2 | ATM |
| ESTRADIOL BENZOATE | 2 | ATM |
| BERZOSERTIB | 2 | ATM |
| LARTESERTIB | 2 | ATM |
| ALTHIAZIDE | 2 | ATM |
Bioactivity and enzyme data
Enzyme cohort genes (≥1 EC): 1.
Cohort genes with ChEMBL bioactivity (full, sorted by assay count)
| Symbol | Assays | Type breakdown |
|---|---|---|
| ATM | 240 | Binding:233, Functional:5, ADMET:2 |
Cohort enzymes (BRENDA EC)
| Symbol | EC numbers | Names |
|---|---|---|
| ATM | 2.7.11.1 | non-specific serine/threonine protein kinase |
Cohort genes with high screening signal
≥100 ChEMBL assays — a studied-ness signal; see Therapeutics for approved-drug status.
| Symbol | ChEMBL assays |
|---|---|
| ATM | 240 |
Pharmacogenomics
Cohort genes with a PharmGKB record: 1; with CPIC/DPWG dosing guidelines: 0.
No cohort gene has a CPIC/DPWG genotype-guided dosing guideline (PharmGKB).
Drug repurposing candidates
30 approved/phased drugs hit cohort targets but don’t yet appear in disease-level clinical trials. Target-inhibition rationale is strongest for cancer driver genes; a bioactivity hit is a screening signal, not a treatment claim.
| Compound | Max phase | Cohort target (bioactivity) |
|---|---|---|
| AMIODARONE HYDROCHLORIDE | 4 | ATM |
| FURAZOLIDONE | 4 | ATM |
| ESTRADIOL ACETATE | 4 | ATM |
| NAFTIFINE HYDROCHLORIDE | 4 | ATM |
| METHYSERGIDE MALEATE | 4 | ATM |
| AMITRIPTYLINE HYDROCHLORIDE | 4 | ATM |
| XYLOMETAZOLINE HYDROCHLORIDE | 4 | ATM |
| FLUVOXAMINE MALEATE | 4 | ATM |
| ESTRADIOL VALERATE | 4 | ATM |
| PERMETHRIN | 4 | ATM |
| MITOTANE | 4 | ATM |
| TICLOPIDINE HYDROCHLORIDE | 4 | ATM |
| ENOXIMONE | 4 | ATM |
| METHYLENE BLUE ANHYDROUS | 4 | ATM |
| DITHIAZANINE IODIDE | 4 | ATM |
| ETHACRYNIC ACID | 4 | ATM |
| SECNIDAZOLE | 4 | ATM |
| MENADIONE | 4 | ATM |
| FENOFIBRATE | 4 | ATM |
| DIPYRIDAMOLE | 4 | ATM |
| DACTOLISIB | 3 | ATM |
| STREPTONIGRIN | 2 | ATM |
| CALCIMYCIN | 2 | ATM |
| ENPIROLINE | 2 | ATM |
| OXACEPROL | 2 | ATM |
| TOLONIUM CHLORIDE | 2 | ATM |
| ESTRADIOL BENZOATE | 2 | ATM |
| BERZOSERTIB | 2 | ATM |
| LARTESERTIB | 2 | ATM |
| ALTHIAZIDE | 2 | ATM |
Druggability pyramid
Cohort genes binned by druggability tier (high → low):
| Tier | Definition | Genes | Symbols |
|---|---|---|---|
| A | Approved (phase 4 drug) | 1 | ATM |
| B | Phased (≥1) drug, not yet approved | 0 | |
| C | Druggable family + PDB, no drug | 0 | |
| D | Druggable family + AlphaFold only, no drug | 0 | |
| E | Difficult family or no structure, no drug | 0 |
Undrugged target profiles
0 cohort genes are undrugged. Ranked by ‘starting-point quality’ (assay depth + drugged-partner adjacency).
Clinical trials & evidence
Clinical trials
Clinical trials: 26.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| PHASE1 | 11 |
| PHASE2 | 8 |
| PHASE1/PHASE2 | 5 |
| PHASE3 | 1 |
| Not specified | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT01231412 | PHASE3 | COMPLETED | Graft-Versus-Host Disease Prophylaxis in Treating Patients With Hematologic Malignancies Undergoing Unrelated Donor Peripheral Blood Stem Cell Transplant |
| NCT04496349 | PHASE2 | RECRUITING | A Study Evaluating APG-115 as a Single Agent or in Combination With APG-2575 in Subjects With R/R T-PLL and NHL |
| NCT06420076 | PHASE1/PHASE2 | RECRUITING | Sequential CAR-T Cells Therapy for CD5/CD7 Positive T-cell Acute Lymphoblastic Leukemia and Lymphoblastic Lymphoma Using CD5/CD7-Specific CAR-T Cells |
| NCT06810778 | PHASE1/PHASE2 | RECRUITING | Duvelisib and Venetoclax in Patients With Relapsed or Refractory Peripheral T-cell Lymphoma (PTCL) |
| NCT07311746 | PHASE1/PHASE2 | NOT_YET_RECRUITING | Phase Ib/II Trial of Cladribine/Ruxolitinib/Venetoclax in Patients With Relapsed/Refractory T-cell Prolymphocytic Leukemia |
| NCT07356245 | PHASE2 | RECRUITING | Ruxolitinib Maintenance Post-Hematopoietic Stem Cell Transplant T-Cell Lymphoma |
| NCT00005803 | PHASE1/PHASE2 | COMPLETED | Autologous Stem Cell Transplant Followed by Donor Stem Cell Transplant in Treating Patients With Relapsed or Refractory Lymphoma |
| NCT00060424 | PHASE2 | COMPLETED | Fludarabine Phosphate and Total-Body Irradiation Before Donor Peripheral Blood Stem Cell Transplant in Treating Patients With Chronic Lymphocytic Leukemia or Small Lymphocytic Leukemia |
| NCT01008462 | PHASE2 | COMPLETED | Autologous Peripheral Blood Stem Cell Transplant Followed by Donor Bone Marrow Transplant in Treating Patients With High-Risk Hodgkin Lymphoma, Non-Hodgkin Lymphoma, Multiple Myeloma, or Chronic Lymphocytic Leukemia |
| NCT01186640 | PHASE2 | COMPLETED | Combined Immunochemotherapy in Patients With T-Prolymphocytic Leukemia (T-PLL) |
| NCT01251575 | PHASE2 | COMPLETED | Sirolimus, Cyclosporine, and Mycophenolate Mofetil in Preventing Graft-versus-Host Disease in Treating Patients With Blood Cancer Undergoing Donor Peripheral Blood Stem Cell Transplant |
| NCT02742727 | PHASE1/PHASE2 | UNKNOWN | CAR-pNK Cell Immunotherapy in CD7 Positive Leukemia and Lymphoma |
| NCT03873493 | PHASE2 | COMPLETED | A Study Evaluating the Efficacy of Venetoclax Plus Ibrutinib in Participants With T-cell Prolymphocytic Leukemia |
| NCT04312841 | PHASE2 | COMPLETED | Letermovir for the Prevention of Cytomegalovirus Reactivation in Patients With Hematological Malignancies Treated With Alemtuzumab |
| NCT04771572 | PHASE1 | RECRUITING | Study of Oral Administration of LP-118 in Patients With Relapsed or Refractory CLL, SLL, MDS, MDS/MPN, AML, CMML-2, MPN-BP, ALL, MF, NHL, RT, MM or T-PLL. |
| NCT05010005 | PHASE1 | RECRUITING | A Study of Ruxolitinib and Duvelisib in People With Lymphoma |
| NCT05377827 | PHASE1 | ACTIVE_NOT_RECRUITING | Dose-Escalation and Dose-Expansion Study to Evaluate the Safety and Tolerability of Anti-CD7 Allogeneic CAR T-Cells (WU-CART-007) in Patients With CD7+ Hematologic Malignancies |
| NCT05823571 | PHASE1 | ACTIVE_NOT_RECRUITING | Itacitinib With High-dose Posttransplantation Cyclophosphamide in Older Patients |
| NCT00749502 | PHASE1 | COMPLETED | A Study of MK4827 in Participants With Advanced Solid Tumors or Hematologic Malignancies (MK-4827-001 AM8) |
| NCT02512497 | PHASE1 | COMPLETED | Romidepsin Maintenance After Allogeneic Stem Cell Transplantation |
| NCT02689453 | PHASE1 | COMPLETED | Subcutaneous Recombinant Human IL-15 (s.c. rhIL-15) and Alemtuzumab for People With Refractory or Relapsed Chronic and Acute Adult T-cell Leukemia (ATL) |
| NCT03989466 | PHASE1 | COMPLETED | Itacitinib and Alemtuzumab in Treating Patients With T-Cell Prolymphocytic Leukemia |
| NCT04526795 | PHASE1 | TERMINATED | Fludarabine, Cytarabine, and Pegcrisantaspase for the Treament of Relapsed or Refractory Leukemia |
| NCT04823091 | PHASE1 | UNKNOWN | Anti-CD7 CAR-Engineered T Cells for T Lymphoid Malignancies Malignancies |
| NCT05225584 | PHASE1 | COMPLETED | Safety, PK, PD, Clinical Activity of KT-333 in Adult Patients With Refractory Lymphoma, Large Granular Lymphocytic Leukemia, Solid Tumors |
| NCT05978141 | Not specified | RECRUITING | A Registry for People With T-cell Lymphoma |
Drugs tested across these trials (top 30)
| Molecule | Max phase | Trials referencing |
|---|---|---|
| FLUDARABINE PHOSPHATE | 4 | 8 |
| DUVELISIB | 4 | 2 |
| CARMUSTINE | 4 | 1 |
| CLADRIBINE | 4 | 1 |
| LETERMOVIR | 4 | 1 |
| NIRAPARIB | 4 | 1 |
| ROMIDEPSIN | 4 | 1 |
| ITACITINIB | 3 | 2 |
| APG-2575 | 2 | 1 |
| INTERLEUKIN 15, RECOMBINANT NON-GLYCOSYLATED | 2 | 1 |
| CHEMBL3805348 | 0 | 2 |
| CHEMBL4538684 | 0 | 2 |
| CHEMBL406352 | 0 | 1 |
| CHEMBL4789656 | 0 | 1 |
| CHEMBL4776881 | 0 | 1 |
| CHEMBL4066465 | 0 | 1 |
Related Atlas pages
- Cohort genes: ATM
- Drugs: Fludarabine Phosphate, Duvelisib, Carmustine, Cladribine, Letermovir, Niraparib, Romidepsin, Itacitinib