tunlametinib (HL-085) / Tianjin Binjiang Pharma |
NCT06008119: Efficacy and Safety of Tunlametinib Plus Vemurafenib in Patients With BRAF V600E-mutant Metastatic Colorectal Cancer |
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| Not yet recruiting | 3 | 165 | NA | Tunlametinib plus Vemurafenib, Doublets Chemotherapy ± Bevacizumab or Doublets Chemotherapy ± Cetuximab | Shanghai Kechow Pharma, Inc. | Colorectal Cancer Metastatic | 12/26 | 12/26 | | |
NCT06008106: Comparing Tunlametinib Capsules and Combination Chemotherapy in Advanced NRAS-mutant Melanoma |
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| Recruiting | 3 | 165 | RoW | tunlametinib, paclitaxel +carboplatin, or temozolomide +cisplatin, or dacarbazine +cisplatin | Shanghai Kechow Pharma, Inc. | Melanoma | 09/27 | 09/27 | | |
| Completed | 2 | 100 | RoW | HL-085 | Shanghai Kechow Pharma, Inc. | Melanoma | 02/23 | 02/23 | | |
NCT05233332: Study of HL-085 and Vemurafinib in Metastatic Colorectal Cancer (mCRC) |
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| Recruiting | 2 | 186 | RoW | HL-085, Vemurafenib, ZELBORAF | Shanghai Kechow Pharma, Inc. | CRC | 01/24 | 07/24 | | |
NCT05263453: HL-085+Vemurafenib to Treat Advanced Melanoma Patients With BRAF V600E/K Mutation |
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| Recruiting | 2 | 104 | RoW | HL-085, Vemurafenib | Shanghai Kechow Pharma, Inc. | Melanoma | 09/24 | 12/24 | | |
NCT05900219: Efficacy and Safety of HL-085 Combined With Vemurafenib in BRAF V600E Patients With Non-small Cell Lung Cancer: a Phase II Clinical Study |
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| Not yet recruiting | 2 | 75 | NA | HL-085+Vemurafenib | Shanghai Kechow Pharma, Inc. | Non-small-cell Lung Cancer | 09/25 | 09/25 | | |
NCT05331105: HL-085 in Adults With Neurofibromatosis Type 1 (NF1) and Inoperable Plexiform Neurofibromas |
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| Recruiting | 2 | 70 | RoW | HL-085 | Shanghai Kechow Pharma, Inc. | Neurofibromatosis 1, Plexiform Neurofibromas | 10/25 | 10/28 | | |
NCT03973151: Study of HL-085 in NRAS Mutant Advanced Melanoma |
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| Completed | 1/2 | 42 | RoW | HL-085 | Shanghai Kechow Pharma, Inc. | Melanoma | 01/21 | 01/21 | | |
NCT04683354: Study of HL-085 in Patients With Advanced Solid Tumor Tumors |
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| Completed | 1 | 28 | US | HL-085 | Kechow Pharma, Inc. | Solid Tumor, Adult | 09/22 | 12/22 | | |
NCT03781219: A PhaseI Study of HL-085 Plus Vemurafenib in Solid Tumor With BRAF V600 Mutation |
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| Recruiting | 1 | 45 | RoW | HL-085, Vemurafenib, ZELBORAF | Shanghai Kechow Pharma, Inc. | Solid Tumor | 12/23 | 12/23 | | |