LBH589
Phase 1CompletedDevelopment Stage
Cancer Patients With Advanced Solid Tumors Including Lymphoma or Chronic Hematological Malignancies
Cancer Patients With Advanced Solid Tumors Including Lymphoma or Chronic Hematological Malignancies
May 1, 2007 → —
About LBH589
LBH589 is a phase 1 stage product being developed by Novartis for Cancer Patients With Advanced Solid Tumors Including Lymphoma or Chronic Hematological Malignancies. The current trial status is completed. This product is registered under clinical trial identifier NCT00472368. Target conditions include Cancer Patients With Advanced Solid Tumors Including Lymphoma or Chronic Hematological Malignancies.
What happened to similar drugs?
20 of 20 similar drugs in Cancer Patients With Advanced Solid Tumors Including Lymphoma or Chronic Hematological Malignancies were approved
Hype Score Breakdown
Clinical Trials (20)
| NCT ID | Phase | Status |
|---|---|---|
| NCT01090973 | Phase 2 | Terminated |
| NCT01007968 | Phase 1 | Completed |
| NCT01065467 | Phase 1 | Completed |
| NCT01013597 | Phase 2 | Completed |
| NCT01032148 | Phase 1 | Terminated |
| NCT01298934 | Phase 1/2 | UNKNOWN |
| NCT00939159 | Phase 2 | Terminated |
| NCT00936611 | Phase 2 | Completed |
| NCT00739414 | Phase 1 | Completed |
| NCT00690677 | Phase 2 | Completed |
| NCT00532675 | Phase 1 | Completed |
| NCT00550277 | Phase 2 | Completed |
| NCT00535951 | Phase 1 | Completed |
| NCT00570284 | Phase 1 | Completed |
| NCT00532389 | Phase 1 | Completed |
| NCT00503451 | Phase 1 | Completed |
| NCT00472368 | Phase 1 | Completed |
| NCT00445068 | Phase 2 | Terminated |
| NCT00449761 | Phase 2 | Terminated |
| NCT00451035 | Phase 2 | Terminated |
Competing Products
20 competing products in Cancer Patients With Advanced Solid Tumors Including Lymphoma or Chronic Hematological Malignancies
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| mFOLFOX regimen + Mitazalimab | Alligator Bioscience AB | Phase 2/3 | 35 |
| Intratumoral Mitazalimab + Intratumoral Nivolumab | Alligator Bioscience AB | Phase 1 | 26 |
| mRNA-2416 | Moderna | Phase 2 | 0 |
| Doxorubicin Hydrochloride Liposome Injection | Dr. Reddy's Laboratories | Phase 1 | 26 |
| E7389 | Eisai | Phase 1 | 29 |
| Veliparib | AbbVie | Phase 2 | 27 |
| AK-105 | Akeso | Phase 1 | 29 |
| XL820 | Exelixis | Phase 1 | 26 |
| Lymphoseek | Navidea Biopharmaceuticals | Phase 3 | 30 |
| Lymphoseek | Navidea Biopharmaceuticals | Phase 3 | 30 |
| ALT-P7 (HM2-MMAE) | Alteogen | Phase 1 | 29 |
| pegylated liposomal doxorubicin (PLD) + PD-1 | CSPC Pharmaceutical Group Limited | Phase 2 | 31 |
| Biomarkers blood, urine and microbiota samples | Eli Lilly | Pre-clinical | 30 |
| gemcitabine + paclitaxel + bevacizumab | Eli Lilly | Phase 2 | 35 |
| pemetrexed | Eli Lilly | Phase 2 | 27 |
| LY3300054 + Prexasertib | Eli Lilly | Phase 1 | 29 |
| BBP-398 with nivolumab | BridgeBio Pharma | Phase 1 | 18 |
| Cetuximab + Oxaliplatin + Capecitabine | Eli Lilly | Phase 2 | 35 |
| Necitumumab + Gemcitabine + Carboplatin | Eli Lilly | Phase 2 | 27 |
| Gemcitabine + Adriamycine + Paclitaxel | Eli Lilly | Phase 2 | 35 |