Vinblastine
drug drugOn this page
Also known as NSC-47842Vinblastina[3h]-vinblastinevinblastin (VBL)vincaleukoblastinevincaleucoblasinevinblastinviblastineVinbllastineSID50125838SID124893649Vinblastine sulfate salt
Summary
Vinblastine (CHEMBL159) is an approved small molecule (ATC L01CA01) targeting TUBB; indicated across 28 conditions including neoplasm and hodgkins lymphoma.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Small molecule
- ATC class: L01CA01
- Targets: 1 (TUBB)
- Indications: 28 conditions
- Clinical trials: 99
- Chemistry: 811 Da · C46H58N4O9
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL159 |
| Name | Vinblastine |
| Type | Small molecule |
| Max phase | 4 |
| FDA approved | yes |
| PubChem CID | 13342 |
| ATC | L01CA01 |
| Molecular formula | C46H58N4O9 |
| Molecular weight | 811 |
| InChIKey | JXLYSJRDGCGARV-CFWMRBGOSA-N |
SMILES: CC[C@@]1(C[C@H]2C[C@@](C3=C(CCN(C2)C1)C4=CC=CC=C4N3)(C5=C(C=C6C(=C5)[C@]78CCN9[C@H]7[C@@](C=CC9)([C@H]([C@@]([C@@H]8N6C)(C(=O)OC)O)OC(=O)C)CC)OC)C(=O)OC)O
IUPAC name: methyl (1R,9R,10S,11R,12R,19R)-11-acetyloxy-12-ethyl-4-[(13S,15R,17S)-17-ethyl-17-hydroxy-13-methoxycarbonyl-1,11-diazatetracyclo[13.3.1.04,12.05,10]nonadeca-4(12),5,7,9-tetraen-13-yl]-10-hydroxy-5-methoxy-8-methyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,13-tetraene-10-carboxylate
Also known as: NSC-47842, Vinblastina, Vinblastine, [3h]-vinblastine, vinblastine, vinblastin (VBL), vincaleukoblastine, vincaleucoblasine, vinblastin, viblastine, Vinblastin, Vinbllastine
Parent form; salt/anhydrous children: CHEMBL378544
Patent coverage: 103,548 distinct patent families (412,636 SureChEMBL compound mentions), from 2 matched compound structure(s). Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.
Targets
Targets
Primary targets (GtoPdb curated mechanism): the Cancer dependency column is the DepMap CRISPR fitness signal (% of screened cell lines dependent on the target).
| Gene | Target | Action | pAffinity | Cancer dependency | UniProt |
|---|---|---|---|---|---|
| TUBB | tubulin beta class I | Inhibition | 9 | P07437 |
Broader ChEMBL bioactivity targets: 21 (assay-derived). Sample: Nuclear receptor ROR-gamma, Solute carrier organic anion transporter family member 1B1, Solute carrier organic anion transporter family member 1B3, ATP-binding cassette sub-family C member 4, Thromboxane-A synthase, Menin/Histone-lysine N-methyltransferase MLL, Tubulin, Tubulin, Tubulin, Prostaglandin G/H synthase 1, Amine oxidase [flavin-containing] B, Multidrug resistance-associated protein 1, Cytochrome P450 3A4, ATP-dependent translocase ABCB1, Proteasome Macropain subunit, Proteasome component C5, ATP-dependent translocase ABCB1, Polyunsaturated fatty acid lipoxygenase ALOX15, Proteasome Macropain subunit MB1, ATP-binding cassette sub-family C member 2.
Bioactivity
ChEMBL activities: 26 potent at pChembl ≥ 5 of 51 total. Top 100 by potency (10 = 0.1 nM, 6 = 1 µM):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| TUBB4A | 7.16 | IC50 | 70 | nM | CHEMBL_ACT_1217712 |
| ABCB1 | 7 | Ki | 100 | nM | CHEMBL_ACT_1285226 |
| TUBB4A | 6.89 | IC50 | 130 | nM | CHEMBL_ACT_25553927 |
| TUBB4A | 6.7 | EC50 | 200 | nM | CHEMBL_ACT_1844115 |
| TUBB4A | 6.52 | IC50 | 300 | nM | CHEMBL_ACT_1838510 |
| Q6B856 | 6.22 | IC50 | 600 | nM | CHEMBL_ACT_15237788 |
| P02550 | 6.22 | IC50 | 600 | nM | CHEMBL_ACT_609098 |
| PTGS1 | 6.21 | AC50 | 623.8 | nM | CHEMBL_ACT_25205427 |
| Q6B856 | 6.16 | IC50 | 700 | nM | CHEMBL_ACT_754323 |
| TUBB4A | 6.13 | IC50 | 740 | nM | CHEMBL_ACT_24730056 |
| P02550 | 5.96 | IC50 | 1100 | nM | CHEMBL_ACT_15702075 |
| ABCB1 | 5.89 | Ki | 1300 | nM | CHEMBL_ACT_1285229 |
| P02550 | 5.8 | IC50 | 1600 | nM | CHEMBL_ACT_5134834 |
| TBXAS1 | 5.73 | IC50 | 1870 | nM | CHEMBL_ACT_7782348 |
| ABCB1 | 5.7 | IC50 | 2000 | nM | CHEMBL_ACT_1183262 |
| ABCB1 | 5.68 | Ki | 2100 | nM | CHEMBL_ACT_11002745 |
| TUBB4A | 5.68 | IC50 | 2100 | nM | CHEMBL_ACT_15185287 |
| ABCB1 | 5.52 | Kd | 3000 | nM | CHEMBL_ACT_11002228 |
| PSMB1 | 5.37 | IC50 | 4280 | nM | CHEMBL_ACT_18537687 |
| PSMB5 | 5.34 | IC50 | 4580 | nM | CHEMBL_ACT_18537721 |
| PSMB2 | 5.31 | IC50 | 4900 | nM | CHEMBL_ACT_18537704 |
| P12530 | 5.3 | IC50 | 5037 | nM | CHEMBL_ACT_7781565 |
| P06795 | 5.1 | IC50 | 8000 | nM | CHEMBL_ACT_11001892 |
| P06795 | 5.1 | IC50 | 8000 | nM | CHEMBL_ACT_1183264 |
| PTGS1 | 5.03 | AC50 | 9252 | nM | CHEMBL_ACT_25206358 |
| ABCB1 | 5 | IC50 | 10000 | nM | CHEMBL_ACT_2049487 |
Target pathways
Aggregated over 1 target gene(s): TUBB.
Top Reactome pathways
24 total, by targets touching each:
| Pathway | Targets | Genes |
|---|---|---|
| Cell Cycle | 1 | TUBB |
| Disease | 1 | TUBB |
| Innate Immune System | 1 | TUBB |
| Immune System | 1 | TUBB |
| Organelle biogenesis and maintenance | 1 | TUBB |
| Regulation of PLK1 Activity at G2/M Transition | 1 | TUBB |
| Loss of Nlp from mitotic centrosomes | 1 | TUBB |
| Recruitment of mitotic centrosome proteins and complexes | 1 | TUBB |
| Loss of proteins required for interphase microtubule organization from the centrosome | 1 | TUBB |
| Centrosome maturation | 1 | TUBB |
| Recruitment of NuMA to mitotic centrosomes | 1 | TUBB |
| Mitotic G2-G2/M phases | 1 | TUBB |
| Cilium Assembly | 1 | TUBB |
| Anchoring of the basal body to the plasma membrane | 1 | TUBB |
| Infectious disease | 1 | TUBB |
| Neutrophil degranulation | 1 | TUBB |
| Mitotic Prometaphase | 1 | TUBB |
| M Phase | 1 | TUBB |
| G2/M Transition | 1 | TUBB |
| Cell Cycle, Mitotic | 1 | TUBB |
| AURKA Activation by TPX2 | 1 | TUBB |
| Potential therapeutics for SARS | 1 | TUBB |
| SARS-CoV Infections | 1 | TUBB |
| Viral Infection Pathways | 1 | TUBB |
Dominant GO biological processes
| GO term | Targets |
|---|---|
| microtubule cytoskeleton organization | 1 |
| mitotic cell cycle | 1 |
| microtubule-based process | 1 |
| cytoskeleton-dependent intracellular transport | 1 |
| natural killer cell mediated cytotoxicity | 1 |
| regulation of synapse organization | 1 |
| spindle assembly | 1 |
| cell division | 1 |
| odontoblast differentiation | 1 |
| cytoskeleton organization | 1 |
Indications & clinical
Indications
13 approved indications. FDA phase 4, plus an anticancer drug’s labelled cancer uses (which ChEMBL often logs at phase 3).
| Indication | Phase | MONDO | EFO |
|---|---|---|---|
| neoplasm | 4 | MONDO:0005070 | EFO:0000616 |
| Hodgkins lymphoma | 3 | MONDO:0004952 | EFO:0000183 |
| cutaneous melanoma | 3 | MONDO:0005012 | EFO:0000389 |
| diffuse large B-cell lymphoma | 3 | MONDO:0018905 | EFO:0000403 |
| leukemia | 3 | MONDO:0005059 | EFO:0000565 |
| lymphoma | 3 | MONDO:0005062 | EFO:0000574 |
| melanoma | 3 | MONDO:0005105 | EFO:0000756 |
| metastatic melanoma | 3 | MONDO:0005191 | EFO:0002617 |
| peripheral T-cell lymphoma, not otherwise specified | 3 | MONDO:0004964 | EFO:0000211 |
| testicular cancer | 3 | MONDO:0005447 | EFO:0004281 |
| lung neoplasm | 3 | MONDO:0021117 | MONDO:0008903 |
| urothelial carcinoma | 3 | MONDO:0040679 | EFO:0008528 |
| skin neoplasm | 3 | MONDO:0002531 | MONDO:0002898 |
9 diseases in clinical trials (phase 1–3, investigational — not approved indications). Highest ChEMBL trial phase per disease; a non-cancer approved use is occasionally logged at phase 3 here.
| Disease (in trials) | Phase | MONDO | EFO |
|---|---|---|---|
| Langerhans cell histiocytosis | 3 | MONDO:0018310 | EFO:1000318 |
| renal cell carcinoma | 2 | MONDO:0005086 | EFO:0000681 |
| acute lymphoblastic leukemia | 2 | MONDO:0004967 | EFO:0000220 |
| acute myeloid leukemia | 2 | MONDO:0018874 | EFO:0000222 |
| brain neoplasm | 2 | MONDO:0021211 | EFO:0003833 |
| neurofibromatosis type 1 | 2 | MONDO:0018975 | MONDO:0018975 |
| paraganglioma | 2 | MONDO:0000448 | EFO:1000453 |
| glioma | 2 | MONDO:0021042 | MONDO:0021637 |
| central nervous system neoplasm | 1 | MONDO:0006130 | EFO:1000158 |
6 further indication records had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.
Clinical trials
Total trials: 99.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE2 | 53 |
| PHASE3 | 26 |
| PHASE1 | 7 |
| PHASE1/PHASE2 | 6 |
| PHASE2/PHASE3 | 2 |
| EARLY_PHASE1 | 2 |
| Not specified | 2 |
| PHASE4 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT06831370 | PHASE4 | RECRUITING | A Study of Brentuximab Vedotin With Doxorubicin, Vinblastine and Dacarbazine in Adults With Hodgkin Lymphoma in India |
| NCT02066220 | PHASE2/PHASE3 | ACTIVE_NOT_RECRUITING | International Society of Paediatric Oncology (SIOP) PNET 5 Medulloblastoma |
| NCT02205762 | PHASE2/PHASE3 | ACTIVE_NOT_RECRUITING | LCH-IV, International Collaborative Treatment Protocol for Children and Adolescents With Langerhans Cell Histiocytosis |
| NCT02670707 | PHASE3 | RECRUITING | Vinblastine/Prednisone Versus Single Therapy With Cytarabine for Langerhans Cell Histiocytosis (LCH) |
| NCT04638790 | PHASE3 | RECRUITING | First Line Chemotherapy for Classical Hodgkin Lymphoma in Russia (HL-Russia-1) |
| NCT04685616 | PHASE3 | RECRUITING | Brentuximab Vedotin in Early Stage Hodgkin Lymphoma |
| NCT06960577 | PHASE3 | RECRUITING | Perioperative Durvalumab With Neoadjuvant ddMVAC or Gemcitabine/Cisplatin in Patients With Muscle-invasive Bladder Cancer (NIAGARA-2) |
| NCT00002495 | PHASE3 | COMPLETED | SWOG-9133 RT w/ or w/o Doxorubicin and Vinblastine in Stage I or Stage II Hodgkin’s Disease |
| NCT00002561 | PHASE3 | COMPLETED | Radiation Therapy and Chemotherapy in Treating Patients With Hodgkin’s Disease |
| NCT00002855 | PHASE3 | COMPLETED | Chemotherapy Plus Hormone Therapy Versus Androgen Suppression in Treating Patients With Metastatic or Unresectable Prostate Cancer |
| NCT00002882 | PHASE3 | COMPLETED | Interferon Alfa With or Without Combination Chemotherapy Plus Interleukin-2 in Treating Patients With Melanoma |
| NCT00003027 | PHASE3 | COMPLETED | Combination Chemotherapy With or Without Interleukin-2 and Interferon Alfa in Treating Patients With Metastatic Melanoma |
| NCT00003376 | PHASE3 | COMPLETED | Two-Drug Combination Chemotherapy Compared With Four-Drug Combination Chemotherapy in Treating Patients With Advanced Cancer of the Urothelium |
| NCT00003389 | PHASE3 | COMPLETED | Combination Chemotherapy With or Without Radiation Therapy in Treating Patients With Hodgkin’s Lymphoma |
| NCT00005047 | PHASE3 | TERMINATED | 4B951, Combination Chemotherapy in Treating Patients With Bladder Cancer |
| NCT00005090 | PHASE3 | TERMINATED | S9901 Combination Chemotherapy With or Without Peripheral Stem Cell Transplantation in Treating Men With Stage III or Stage IV Hodgkin’s Disease |
| NCT00006237 | PHASE3 | COMPLETED | S0008: Chemotherapy Plus Biological Therapy in Treating Patients With Melanoma |
| NCT00024167 | PHASE3 | TERMINATED | Chemotherapy With or Without Strontium-89 in Treating Patients With Prostate Cancer |
| NCT00038558 | PHASE3 | COMPLETED | Prophylactic Use of Filgrastim SD/01 in Patients With Hodgkin’s Disease Receiving ABVD Chemotherapy |
| NCT00072215 | PHASE3 | TERMINATED | Cisplatin and Ifosfamide Combined With Either Paclitaxel or Vinblastine in Treating Men With Progressive or Recurrent Metastatic Germ Cell Tumors |
| NCT00264953 | PHASE3 | COMPLETED | HD11 for Intermediate Stages |
| NCT00265018 | PHASE3 | COMPLETED | HD10 for Early Stages |
| NCT00488605 | PHASE3 | WITHDRAWN | H-9926-LCH III: Treatment Protocol of the Third International Study for Langerhans Cell Histiocytosis |
| NCT01134861 | PHASE3 | COMPLETED | Radiation Therapy Plus Chemotherapy in Treating Patients With Non-small Cell Lung Cancer |
| NCT01148446 | PHASE3 | COMPLETED | R-CHOP Versus R-mini-CEOP in Elderly Patients(>65)With DLBCL |
| NCT01251107 | PHASE3 | COMPLETED | Study Comparing ABVD vs BEACOPP in Advanced Hodgkin’s Lymphoma |
| NCT01356680 | PHASE3 | COMPLETED | HD17 for Intermediate Stage Hodgkin Lymphoma |
| NCT01712490 | PHASE3 | COMPLETED | A Frontline Therapy Trial in Participants With Advanced Classical Hodgkin Lymphoma |
| NCT03159897 | PHASE3 | COMPLETED | FIL Study on ABVD DD-DI as Upfront Therapy in HL. |
| NCT02840409 | PHASE2 | ACTIVE_NOT_RECRUITING | Vinblastine +/- Bevacizumab in Children With Unresectable or Progressive Low Grade Glioma (LGG) |
| NCT02979522 | PHASE1/PHASE2 | ACTIVE_NOT_RECRUITING | A Study of Brentuximab Vedotin + Adriamycin, Vinblastine, and Dacarbazine in Pediatric Participants With Advanced Stage Newly Diagnosed Hodgkin Lymphoma |
| NCT03033914 | PHASE1/PHASE2 | ACTIVE_NOT_RECRUITING | A(B)VD Followed by Nivolumab as Frontline Therapy for Higher Risk Patients With Classical Hodgkin Lymphoma (HL) |
| NCT03233347 | PHASE2 | ACTIVE_NOT_RECRUITING | Doxorubicin, Vinblastine, Dacarbazine, Brentuximab Vedotin, and Nivolumab in Treating Patients With Stage I-II Hodgkin Lymphoma |
| NCT03407144 | PHASE2 | ACTIVE_NOT_RECRUITING | Safety and Efficacy of Pembrolizumab (MK-3475) in Children and Young Adults With Classical Hodgkin Lymphoma (MK-3475-667/KEYNOTE-667) |
| NCT03517137 | PHASE2 | ACTIVE_NOT_RECRUITING | Very Early PET-response Adapted Targeted Therapy for Advanced Hodgkin Lymphoma: a Single -Arm Phase II Study |
| NCT03712202 | PHASE2 | ACTIVE_NOT_RECRUITING | Brentuximab Vedotin and Nivolumab in Treating Patients With Early Stage Classic Hodgkin Lymphoma |
| NCT03755804 | PHASE2 | ACTIVE_NOT_RECRUITING | Pediatric Classical Hodgkin Lymphoma Consortium Study: cHOD17 |
| NCT05137262 | PHASE2 | ACTIVE_NOT_RECRUITING | A Phase II Multicenter Study of Chemotherapy Versus Chemotherapy Plus Durvalumab (MEDI 4736) in Patients With Lymph Node Positive Urothelial Carcinoma of the Bladder |
| NCT05180825 | PHASE2 | RECRUITING | Pediatric Low Grade Glioma - MEKinhibitor TRIal vs Chemotherapy |
| NCT05404945 | PHASE2 | ACTIVE_NOT_RECRUITING | Fitness-adapted, Pembrolizumab-based Therapy for Untreated Classical Hodgkin Lymphoma Patients 60 Years of Age and Above |
| NCT06164275 | PHASE2 | ACTIVE_NOT_RECRUITING | Pembrolizumab Followed by Chemotherapy for the Treatment of Patients With Classical Hodgkin Lymphoma |
| NCT06377566 | PHASE2 | RECRUITING | A Study of BV-AVD in People With Bulky Hodgkin Lymphoma |
| NCT06745076 | PHASE2 | RECRUITING | Personalized Reduction of Chemotherapy Intensity Through ctDNA Evaluation for the Treatment of Patients With Advanced Hodgkin Lymphoma |
| NCT06984146 | PHASE2 | RECRUITING | Nivo40-AVD for Advanced Classic Hodgkin Lymphoma |
| NCT07013565 | PHASE2 | RECRUITING | Chemoimmunotherapy for ALK+ Relapsed/Refractory ALCL |
| NCT07551583 | PHASE2 | NOT_YET_RECRUITING | Phase 2 Study Of Nivolumab Plus AVD In Pediatric, Adolescent, And Young Adult Patients With CHL |
| NCT00002715 | PHASE2 | COMPLETED | Combination Chemotherapy in Treating Patients With Advanced Hodgkin’s Lymphoma |
| NCT00003084 | PHASE2 | COMPLETED | Combination Chemotherapy With Ketoconazole in Treating Patients With Prostate Cancer |
| NCT00030264 | PHASE2 | COMPLETED | Combination Chemotherapy in Treating Patients With Neurofibromatosis and Progressive Plexiform Neurofibromas |
| NCT00086801 | PHASE2 | COMPLETED | Combination Chemotherapy in Treating Patients With Newly Diagnosed Stage I or Stage II Hodgkin’s Lymphoma |
| NCT00147875 | PHASE1/PHASE2 | COMPLETED | Study of Prednisone, Vinblastine, Doxorubicin, and Gemcitabine in Elderly Patients With Advanced Stages Hodgkin’s Lymphoma |
| NCT00186875 | PHASE2 | COMPLETED | Therapy for Pediatric Relapsed or Refractory Acute Lymphoblastic Leukemia |
| NCT00215046 | PHASE2 | COMPLETED | Vinblastine and Methotrexate in Children With Pulmonary Vein Stenosis |
| NCT00225173 | PHASE2 | TERMINATED | Combination Chemotherapy +/- Radiation in High Risk Hodgkin’s Disease |
| NCT00352027 | PHASE2 | COMPLETED | Chemotherapy With Low-Dose Radiation for Pediatric Hodgkin Lymphoma |
| NCT00369681 | PHASE2 | COMPLETED | Phase 2 Study of Rituximab-ABVD in Classical Hodgkin Lymphoma |
| NCT00504504 | PHASE2 | COMPLETED | Rituximab and ABVD for Hodgkin’s Patients |
| NCT00512980 | PHASE2 | TERMINATED | PVAG-14 Pilot for Intermediate Stages Hodgkin Lymphoma |
| NCT00516750 | PHASE2 | TERMINATED | Gene Expression Profiling in Patients With Invasive Bladder Cancer Receiving Methotrexate, Vinblastine, Doxorubicin, and Cisplatin |
| NCT00520403 | PHASE2 | COMPLETED | A Study of Avastin (Bevacizumab) in Combination With Standard Therapy in Patients With Metastatic Renal Cell Cancer. |
| NCT00635726 | PHASE2 | TERMINATED | Methotrexate, Vinblastine, Doxorubicin and Cisplatin (MVAC) Followed by Gemcitabine Plus Cisplatin (GEM+CDDP) in Locally Advanced or Metastatic Bladder Cancer |
| NCT00654732 | PHASE2 | COMPLETED | Combination Chemotherapy With or Without Rituximab in Treating Participants With Stage III-IV Classic Hodgkin Lymphoma |
| NCT00808639 | PHASE2 | COMPLETED | Dose-Dense MVAC With Pegfilgrastim Support in Subjects With Muscle-Invasive Urothelial Carcinoma |
| NCT00885534 | PHASE2 | COMPLETED | Genetic Variates of Response to Cisplatin, Vinblastine, and Temozolomide (CVT) in Patients With Metastatic Melanoma |
| NCT01285817 | PHASE2 | COMPLETED | A Clinical Trial Using Metronomic Oral Low-dose Cyclophosphamide Alternating With Low-dose Oral Methotrexate With Continuous Celecoxib and Weekly Vinblastine in Children and Adolescents With Relapsed or Progressing soliD Tumours. |
| NCT01390584 | PHASE2 | TERMINATED | Chemotherapy Based on PET Scan in Treating Patients With Stage I or Stage II Hodgkin Lymphoma |
| NCT01468740 | PHASE2 | UNKNOWN | Prospective Study on HIV-related Hodgkin Lymphoma |
| NCT01476410 | PHASE2 | COMPLETED | Brentuximab Vedotin and Combination Chemotherapy in Treating Older Patients With Previously Untreated Stage II-IV Hodgkin Lymphoma |
| NCT01542255 | PHASE2 | TERMINATED | Metronomic Therapy in Patients With Metastatic Melanoma |
| NCT01639521 | PHASE2 | WITHDRAWN | Gemcitabine Hydrochloride and Cisplatin or High-Dose Methotrexate, Vinblastine, Doxorubicin Hydrochloride, and Cisplatin in Treating Patients With Urothelial Cancer |
| NCT01700946 | PHASE2 | COMPLETED | Therapy for Pediatric Relapsed or Refractory Precursor B-Cell Acute Lymphoblastic Leukemia and Lymphoma |
| NCT01771107 | PHASE1/PHASE2 | COMPLETED | Brentuximab Vedotin and Combination Chemotherapy in Treating Patients With Stage II-IV HIV-Associated Hodgkin Lymphoma |
| NCT01887522 | PHASE2 | TERMINATED | Study of Vinblastine in Combination With Nilotinib in Children, Adolescents, and Young Adults |
| NCT02177695 | PHASE2 | COMPLETED | S1314, Co-expression Extrapolation (COXEN) Program to Predict Chemotherapy Response in Patients With Bladder Cancer |
| NCT02181738 | PHASE2 | COMPLETED | Study of Nivolumab in Patients With Classical Hodgkin’s Lymphoma (Registrational) |
| NCT02292979 | PHASE2 | COMPLETED | Brentuximab Vedotin Associated With Chemotherapy in Untreated Patients With Hodgkin Lymphoma. |
| NCT02412670 | PHASE2 | COMPLETED | Chemotherapy Before Surgery in Treating Patients With High Grade Upper Urinary Tract Cancer |
| NCT02414568 | PHASE2 | COMPLETED | Bendamustine Study in Classical Hodgkin Lymphoma Patients Over 60 Treated by Prednisone, Vinblastine and Doxorubicin |
| NCT02710734 | PHASE2 | COMPLETED | Risk Enabled Therapy After Initiating Neoadjuvant Chemotherapy for Bladder Cancer (RETAIN) |
| NCT03004833 | PHASE2 | COMPLETED | Nivolumab and AVD in Early-stage Unfavorable Classical Hodgkin Lymphoma |
| NCT03331341 | PHASE1/PHASE2 | COMPLETED | Doxorubicin Hydrochloride, Pembrolizumab, Vinblastine, and Dacarbazine in Treating Patients With Classical Hodgkin Lymphoma |
| NCT03527628 | PHASE2 | UNKNOWN | OPTmizing Advanced Stage HodgkIn LymphoMa patIentS Therapy |
| NCT03580408 | PHASE2 | COMPLETED | Study Of Nivolumab Alone, Or In Combination With Vinblastin In Patients With Classical Hodgkin Lymphoma |
| NCT03585465 | PHASE1/PHASE2 | TERMINATED | Nivolumab in Combination With Metronomic Chemotherapy in Paediatrics Refractory / Relapsing Solid Tumors |
| NCT03646123 | PHASE2 | TERMINATED | Clinical Trial of Brentuximab Vedotin in Classical Hodgkin Lymphoma |
| NCT03912818 | PHASE2 | TERMINATED | Durvalumab and Standard Chemotherapy Before Surgery in Treating Patients With Variant Histology Bladder Cancer |
| NCT05008224 | PHASE2 | COMPLETED | Study of Safety and Efficacy of Pembrolizumab and Chemotherapy in Participants With Newly Diagnosed Classical Hodgkin Lymphoma (cHL) (MK-3475-C11/KEYNOTE-C11) |
| NCT05062278 | PHASE2 | UNKNOWN | Vinblastine for Leukoreduction in Newly Diagnosed AML and Hyperleukocytosis |
| NCT00001570 | PHASE1 | COMPLETED | A Phase I Study of Continuous Intravenous Infusion of PSC 833 and Vinblastine in Patients With Metastatic Renal Cancer |
| NCT00498979 | PHASE1 | COMPLETED | Sodium Stibogluconate and IFNa-2b Followed By CDDP, VLB and DTIC Treating Pts.With Advanced Melanoma or Other Cancers |
| NCT01056679 | PHASE1 | COMPLETED | Adriamycin, Vinblastine, DTIC and Revlimid in Elderly Hodgkin Lymphoma Patients |
| NCT01060904 | PHASE1 | COMPLETED | A Phase 1 Study of Brentuximab Vedotin Combined With Multi-Agent Chemotherapy for Hodgkin Lymphoma |
| NCT01135563 | PHASE1 | COMPLETED | Study of Vinblastine and Sirolimus in Children With Recurrent/Refractory Solid Tumours Including CNS Tumours |
| NCT01884922 | PHASE1 | COMPLETED | Study Of Vinblastine in Combination With Nilotinib in Children, Adolescents and Young Adults |
| NCT02343718 | PHASE1 | COMPLETED | Vinblastine and Temsirolimus in Pediatrics With Recurrent or Refractory Lymphoma or Solid Tumours Including CNS Tumours |
| NCT06204614 | EARLY_PHASE1 | ENROLLING_BY_INVITATION | Drug Screening Using IMD in Bladder Cancer |
| NCT06381570 | EARLY_PHASE1 | RECRUITING | Pilot Study of Vinblastine and Tovorafenib in Pediatric Patients With Recurrent/Progressive RAF Altered Low Grade Gliomas |
| NCT00187057 | Not specified | COMPLETED | Study for Treatment of Cancer in Children With Ataxia-telangiectasia |
| NCT00187070 | Not specified | COMPLETED | Large Cell Lymphoma Pilot Study III |
Clinical evidence (CIViC)
No CIViC predictive evidence (expected for non-precision-medicine drugs).
Pharmacology
Pharmacogenomics
No PharmGKB pharmacogenomic data curated for this drug.
Related molecules
Related molecules
Molecules sharing ≥1 of this drug’s curated primary targets, merged from two biobtree sources and ranked by shared-target count, then clinical phase: ChEMBL clinical-stage candidates (development phase ≥2) and PubChem drug-class bioactivity (approved / known drugs acting on the target). Deduplicated by drug name; the drug’s own salt forms are excluded. Note: for a drug with few primary targets a shared-target match can reflect off-target / promiscuous binding rather than the same therapeutic mechanism — the phase ordering surfaces bona-fide therapeutics first.
17 molecules share ≥1 primary target. Top 17 by shared-target count:
| Molecule | Source | Status | Shared targets |
|---|---|---|---|
| PODOFILOX | ChEMBL + PubChem | Phase 4 (approved) | TUBB |
| COLCHICINE | ChEMBL | Phase 4 (approved) | TUBB |
| DOCETAXEL | ChEMBL | Phase 4 (approved) | TUBB |
| LEVOFLOXACIN | ChEMBL | Phase 4 (approved) | TUBB |
| NOSCAPINE | ChEMBL | Phase 4 (approved) | TUBB |
| PACLITAXEL | ChEMBL | Phase 4 (approved) | TUBB |
| TIRBANIBULIN | ChEMBL | Phase 4 (approved) | TUBB |
| VINCRISTINE | ChEMBL | Phase 4 (approved) | TUBB |
| VINORELBINE | ChEMBL | Phase 4 (approved) | TUBB |
| PATUPILONE | ChEMBL | Phase 3 | TUBB |
| ABT-751 | ChEMBL | Phase 2 | TUBB |
| DOLASTATIN-10 | ChEMBL | Phase 2 | TUBB |
| INDIBULIN | ChEMBL | Phase 2 | TUBB |
| MAYTANSINE | ChEMBL | Phase 2 | TUBB |
| MOLIBRESIB | ChEMBL | Phase 2 | TUBB |
| NOCODAZOLE | ChEMBL | Phase 2 | TUBB |
| PARBENDAZOLE | ChEMBL | Phase 2 | TUBB |
Related Atlas pages
- Genes: TUBB
- Indicated for: neoplasm, Hodgkins lymphoma, cutaneous melanoma, diffuse large B-cell lymphoma, leukemia, lymphoma, melanoma, metastatic melanoma, peripheral T-cell lymphoma, not otherwise specified, testicular cancer, lung neoplasm, urothelial carcinoma, skin neoplasm
- In clinical trials for: Langerhans cell histiocytosis, renal cell carcinoma, acute lymphoblastic leukemia, acute myeloid leukemia, brain neoplasm, neurofibromatosis type 1, paraganglioma, glioma
- Drugs: Podofilox, Colchicine, Docetaxel, Levofloxacin, Noscapine, Paclitaxel, Tirbanibulin, Vincristine, Vinorelbine, Patupilone