Dr. Reddy's bevacizumab
Bevacizumab biosimilar developed by Dr. Reddy's Laboratories. Reference product Avastin.
About Dr. Reddy's bevacizumab
Dr. Reddy's received its bevacizumab permission in India in 2018, with a separate permission for the drug substance in 2022 and liver cancer added in 2026. It is one of the more complete Indian bevacizumab labels.
Status by market
United States
Not listed by FDA.
European Union
Not listed by EMA.
United Kingdom
Not listed by MHRA.
Japan
Not listed by PMDA.
Canada
Not listed by HC.
India
Central Drugs Standard Control OrganisationApprovedUnited Arab Emirates
Not listed by EDE.
Other developers in the same markets
Where Dr. Reddy's bevacizumab holds an approval, these are the other bevacizumab biosimilars approved in that market.
| Market | Rivals | Developers (product) |
|---|---|---|
| CDSCO | 7 | Biocon Biologics (Jobevne / Abevmy / Krabeva), CuraTeQ Biologics (CuraTeQ bevacizumab), Enzene Biosciences (Enzene Biosciences bevacizumab), Hetero (Hetero bevacizumab), Intas Pharmaceuticals (Intas bevacizumab), Reliance Life Sciences (Reliance Life Sciences bevacizumab), Zydus Lifesciences (Zydus bevacizumab) |
Same developer, other molecules
Other biosimilars in the Atlas developed by Dr. Reddy's Laboratories: Dr. Reddy's darbepoetin alfa, Dr. Reddy's pegfilgrastim, Dr. Reddy's trastuzumab, Teriparatide Dr. Reddy's, Zimrixby / Ituxredi.
Chronology
- CDSCOSep 2018CDSCO permission granted
Sources
S014CDSCO, permissions granted in Form 46 and 46A, to 2019 Primary (regulator)
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