Viatris

Biosimilar developer, United States. 2 development products across 2 molecules: bevacizumab, darbepoetin alfa.

First approval in the Atlas: Sep 2019, Darbepoetin Alfa BS MYL, darbepoetin alfa (PMDA)
FDAproducts approved0
EMAproducts approved0
MHRAproducts approved0
PMDAproducts approved1
HCproducts approved0
CDSCOproducts approved0
EDEproducts registered0

Portfolio by market

MoleculeProductFDAEMAMHRAPMDAHCCDSCOEDEMarkets
BevacizumabLextemy·withdrawn·····0/7
Darbepoetin alfaDarbepoetin Alfa BS MYL···Sep 2019···1/7

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

Also holds or markets

Products developed by another company for which Viatris is the licence holder or applicant in one or more markets.

MoleculeBrandMarketHolder or applicantApprovedDeveloper
EtanerceptMylan Pharmaceuticals Private (INN only)CDSCOMylan Pharmaceuticals Private Limited, now Biocon Biologics LimitedJan 2021Lupin

In development

ClinicalTrials.gov lists two comparative trials sponsored by Viatris for one molecule: adalimumab. Candidates without an approval yet in the seven markets: BMO-2.

MoleculeCandidateDeveloper or sponsorReference productPhaseDesignRegistry statusStartedPrimary completionIn the AtlasRegistry record
AdalimumabBMO-2ViatrisHumiraPhase 1Comparative PKCompletedDec 2014May 2015no approval in the seven marketsNCT02472912
AdalimumabMYL-1401AViatrisHumiraPhase 3Comparative efficacyCompletedJun 2015May 2016HulioNCT02714322

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 Viatris, by number of shared molecules. Overlap is the clearest sign of who competes with whom for the same tenders and licensing partners.

Chronology

Compare Viatris with other developers on the comparison page.

Considering a partner, a licence or a new market for a biosimilar portfolio? EvySaif's regulatory strategy and value dossier work covers the regulatory and market-access side of that decision.

Planning your biosimilar strategy?

EvySaif can help assess your regulatory pathway, clinical evidence requirements and market-entry strategy across India, UAE and other target markets.

Talk to a biosimilar regulatory consultant
Data current to September 2026.