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Dr. Reddy's Laboratories

Biosimilar developer, India. 6 development products across 6 molecules: bevacizumab, darbepoetin alfa, pegfilgrastim, rituximab, teriparatide, trastuzumab.

First approval in the Atlas: Mar 2010, Dr. Reddy's Laboratories (INN only), darbepoetin alfa (CDSCO)
FDAproducts approved1
EMAproducts approved1
MHRAproducts approved2
PMDAproducts approved0
HCproducts approved0
CDSCOproducts approved4
EDEproducts registered0

About Dr. Reddy's Laboratories

Dr. Reddy's launched Reditux, widely regarded as the world's first rituximab biosimilar, in India in 2007, before the published permission lists begin. It holds the first darbepoetin permission in the world, from 2010, and Indian permissions for pegfilgrastim, trastuzumab and bevacizumab. In 2024 its rituximab was approved in Europe as Ituxredi and in 2026 in the United States as Zimrixby, the first rituximab from an Indian developer in either market.

Portfolio by market

MoleculeProductFDAEMAMHRAPMDAHCCDSCOEDEMarkets
BevacizumabDr. Reddy's bevacizumab·····Sep 2018·1/7
Darbepoetin alfaDr. Reddy's darbepoetin alfa·····Mar 2010·1/7
PegfilgrastimDr. Reddy's pegfilgrastim·····Jan 2011·1/7
RituximabZimrixby / Ituxredi DRL_RIJul 2026Sep 2024MHRA····3/7
TeriparatideTeriparatide Dr. Reddy's··MHRA····1/7
TrastuzumabDr. Reddy's trastuzumab·····Mar 2018·1/7

Month shown is the first approval or registration of that product in that market.

In development

ClinicalTrials.gov lists three comparative trials sponsored by Dr. Reddy's Laboratories for two molecules: abatacept, rituximab. Candidates without an approval yet in the seven markets: DRL_AB.

MoleculeCandidateDeveloper or sponsorReference productPhaseDesignRegistry statusStartedPrimary completionIn the AtlasRegistry record
AbataceptDRL_ABDr. Reddy's LaboratoriesOrenciaPhase 1Comparative PKUnknown, last recruitingOct 2023Apr 2024no approval in the seven marketsNCT06126042
RituximabDRL_RIDr. Reddy's LaboratoriesMabTheraPhase 3Comparative efficacyCompletedApr 2020Jan 2022Zimrixby / ItuxrediNCT04268771
RituximabDRL_RIDr. Reddy's LaboratoriesMabTheraPhase 3Comparative efficacyCompletedMay 2019Sep 2022Zimrixby / ItuxrediNCT03976102

Registry data from ClinicalTrials.gov, entered by the sponsors and not verified by any regulator. Status and dates are as posted; sponsors often update them late. Trials registered only on other registries, such as India's CTRI or China's ChiCTR, are not included. Checked 12 Sep 2026.

Companies on the same molecules

Developers whose portfolios overlap most with Dr. Reddy's Laboratories, by number of shared molecules. Overlap is the clearest sign of who competes with whom for the same tenders and licensing partners.

Chronology

Compare Dr. Reddy's Laboratories with other developers on the comparison page.

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Data current to September 2026.