Drugs that contain Dabrafenib Mesylate
1. Drug name - TAFINLAR
| Patent Number | Company | Patent Title | Patent Expiry | Activity Alert |
|---|---|---|---|---|
| These patents protects the active chemical substance. Only patent owner can launch products that use this active substance. | ||||
| US8415345 | NOVARTIS | Benzene sulfonamide thiazole and oxazole compounds |
Jan, 2030
(7 years from now) | |
| US7994185 | NOVARTIS | Benzene sulfonamide thiazole and oxazole compounds |
Jan, 2030
(7 years from now) | |
| US8703781 | NOVARTIS | Pharmaceutical combination of MEK inhibitor and B-RAF inhibitors |
Oct, 2030
(8 years from now) | |
| CN102083312A | NOVARTIS | Benzene Sulfonamide Thiazole And Oxazole Compounds |
May, 2029
(6 years from now) | |
| CN102083312B | NOVARTIS | Benzene Sulfonamide Thiazole And Oxazole Compounds |
May, 2029
(6 years from now) | |
| CN102655753A | NOVARTIS | Combination |
Oct, 2030
(8 years from now) | |
| CN102655753B | NOVARTIS | Combined Medicine |
Oct, 2030
(8 years from now) | |
| IN275655B | NOVARTIS | Benzene Sulfonamide Thiazole And Oxazole Compounds |
May, 2029
(6 years from now) | |
| IN201004199P2 | NOVARTIS | Benzene Sulfonamide Thiazole And Oxazole Compounds |
May, 2029
(6 years from now) | |
| EP2282636A4 | NOVARTIS | Benzene Sulfonamide Thiazole And Oxazole Compounds |
May, 2029
(6 years from now) | |
| EP2282636B1 | NOVARTIS | Benzene Sulfonamide Thiazole And Oxazole Compounds |
May, 2029
(6 years from now) | |
| EP2282636A2 | NOVARTIS | Benzene Sulfonamide Thiazole And Oxazole Compounds |
May, 2029
(6 years from now) | |
| EP2488033A1 | NOVARTIS | Combination Comprising An Mek Inhibitor And A B-Raf Inhibitor |
Oct, 2030
(8 years from now) | |
| EP2488033B1 | NOVARTIS | Combination Comprising An Mek Inhibitor And A B-Raf Inhibitor |
Oct, 2030
(8 years from now) | |
| EP2488033A4 | NOVARTIS | Combination |
Oct, 2030
(8 years from now) | |
| These patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc). | ||||
| US8835443 | NOVARTIS | Pyrimidine compound and medical use thereof |
Jun, 2025
(2 years from now) | |
| US9233956 | NOVARTIS | Benzene sulfonamide thiazole and oxazole compounds |
May, 2029
(6 years from now) | |
| US8952018 | NOVARTIS | Pharmaceutical combination of MEK inhibitor and B-Raf inhibitors |
Oct, 2030
(8 years from now) | |
| US10869869 | NOVARTIS | Method of adjuvant cancer treatment |
Aug, 2033
(10 years from now) | |
Treatment: Tafinlar(r) is indicated, in combination with trametinib, for the treatment of patients with metastatic non-small cell lung cancer (nsclc) with braf v600e mutation as detected by an fda-approved test.; tafinlar is indicated, in combination with trametinib, for the treatment of patients with locally advanced or metastatic anaplastic thyroid cancer (atc) with braf v600e mutation and with no satisfactory locoregional treatment options; tafinlar(r) is indicated, in combination with trametinib, for the treatment of patients with unresectable or metastatic melanoma with braf v600e or v600k mutations, as detected by an fda-approved test.; tafinlar is indicated, in combination with trametinib, for the adjuvant treatment of patients with melanoma with braf v600e or v600k mutations, as detected by an fda-approved test, and involvement of lymph node(s), following complete resection; Tafinlar is indicated, in combination with trametinib, for the treatment of patients with unresectable or metastatic melanoma with braf v600e or v600k mutations, as detected by an fda-approved test.; tafinlar is indicated, in combination with trametinib, for the adjuvant treatment of patients with melanoma with braf v600e or v600k mutations, as detected by an fda-approved test, and involvement of lymph node(s), following complete resection; treatment of patients with unresectable or metastatic melanoma with braf v600e mutations after confirming the presence of braf v600e mutation; tafinlar is indicated as a single agent for the treatment of patients with unresectable or metastatic melanoma with braf v600e mutation as detected by an fda-approved test; Tafinlar(r) is indicated, in combination with trametinib, for the treatment of patients with metastatic non-small cell lung cancer (nsclc) with braf v600e mutation as detected by an fda-approved test.; Tafinlar(r) is indicated, in combination with trametinib, for the adjuvant treatment of patients with melanoma with braf v600e or v600k mutations as detected by an fda-approved test, and involvement of lymph node(s), following complete resection
Dosage: CAPSULE;ORAL
| Strength | Dosage | Availability |
|---|---|---|
| EQ 50MG BASE | CAPSULE;ORAL | Prescription |
| EQ 75MG BASE | CAPSULE;ORAL | Prescription |
availability in other generic markets.
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