Global InformationPolatuzumab vedotin information
| Monoclonal antibody | |
|---|---|
| Type | Whole antibody |
| Source | Humanized (from mouse) |
| Target | CD79B |
| Clinical data | |
| Trade names | Polivy |
| Other names | DCDS4501A, RG7596, polatuzumab vedotin-piiq |
| AHFS/Drugs.com | Monograph |
| MedlinePlus | a619039 |
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| Formula | C6670H10317N1745O2087S40 |
| Molar mass | 149627.43 g·mol−1 |
Polatuzumab vedotin, sold under the brand name Polivy, is a CD79b-directed antibody-drug conjugate medication used for the treatment of diffuse large B-cell lymphoma (cancer).[6] It was developed by the Genentech subsidiary of Roche.[8]
The most common side effects include low levels of white blood cells (neutropenia), platelets (thrombocytopenia) and red blood cells (anemia); nerve damage (peripheral neuropathy); fatigue; diarrhea; fever; decreased appetite; and pneumonia.[9]
Polatuzumab vedotin was approved for medical use in the United States in June 2019,[9][10][11] in Australia in October 2019,[1] in the European Union in January 2020,[7] and in Canada in November 2020.[3]
- ^ a b c "Polivy Australian prescription medicine decision summary". Therapeutic Goods Administration (TGA). 13 December 2019. Archived from the original on 5 March 2020. Retrieved 23 August 2020.
- ^ a b https://www.guildlink.com.au/gc/ws/ro/pi.cfm?product=roppoliv11019 Archived 9 January 2023 at the Wayback Machine [bare URL]
- ^ a b "Summary Basis of Decision (SBD) for Polivy". Health Canada. 23 October 2014. Archived from the original on 30 May 2022. Retrieved 29 May 2022.
- ^ "Polivy 30 mg powder for concentrate for solution for infusion - Summary of Product Characteristics (SmPC)". (emc). 20 July 2022. Retrieved 22 April 2023.
- ^ "Polivy 140 mg powder for concentrate for solution for infusion - Summary of Product Characteristics (SmPC)". (emc). 20 July 2022. Retrieved 22 April 2023.
- ^ a b "Polivy- polatuzumab vedotin injection, powder, lyophilized, for solution". DailyMed. 14 November 2019. Archived from the original on 22 October 2020. Retrieved 23 August 2020.
- ^ a b Cite error: The named reference
Polivy EPARwas invoked but never defined (see the help page). - ^ "FDA Grants Genentech's Polivy Accelerated Approval for People With Previously Treated Aggressive Lymphoma" (Press release). Genentech. 10 June 2019. Archived from the original on 17 February 2023. Retrieved 22 April 2023.
- ^ a b "FDA approves first chemoimmunotherapy regimen for patients with relapsed or refractory diffuse large B-cell lymphoma" (Press release). U.S. Food and Drug Administration (FDA). 10 June 2019. Archived from the original on 25 November 2019. Retrieved 24 November 2019.
This article incorporates text from this source, which is in the public domain.
- ^ "Drug Approval Package: Polivy". U.S. Food and Drug Administration (FDA). 2 July 2019. Archived from the original on 30 October 2020. Retrieved 8 March 2020.
- ^ "Drug Trials Snapshots: Polivy". U.S. Food and Drug Administration (FDA). 17 June 2019. Archived from the original on 25 November 2019. Retrieved 24 November 2019. This article incorporates text from this source, which is in the public domain.
