Pfizer
Biosimilar developer, United States. 7 development products across 7 molecules: adalimumab, bevacizumab, filgrastim, infliximab, pegfilgrastim, rituximab, trastuzumab.
About Pfizer
Pfizer's biosimilar range is built around three cancer antibodies, rituximab, trastuzumab and bevacizumab, sold as Ruxience, Trazimera and Zirabev, and the growth factors filgrastim and pegfilgrastim from its Hospira unit. Seven molecules are approved in the United States, Europe and Canada, four in Japan under Pfizer's own name, and four registered in the UAE. Pfizer also sells Celltrion's infliximab in the United States and India, and never launched its own.
Portfolio by market
| Molecule | Product | FDA | EMA | MHRA | PMDA | HC | CDSCO | EDE | Markets |
|---|---|---|---|---|---|---|---|---|---|
| Adalimumab | Abrilada / Amsparity PF-06410293 | Nov 2019 | Feb 2020 | · | · | Jan 2021 | · | · | 3/7 |
| Bevacizumab | Zirabev PF-06439535 | Jun 2019 | Feb 2019 | MHRA | Jun 2019 | Jun 2019 | · | Dec 2020 | 6/7 |
| Filgrastim | Nivestym / Nivestim PF-06881893 | Jul 2018 | Jun 2010 | MHRA | · | Apr 2020 | · | · | 4/7 |
| Infliximab | Ixifi / Zessly PF-06438179 (GP1111) | Dec 2017 | May 2018 | MHRA | Jul 2018 | Dec 2021 | · | · | 5/7 |
| Pegfilgrastim | Nyvepria PF-06881894 | Jun 2020 | Nov 2020 | · | · | Oct 2020 | · | May 2024 | 4/7 |
| Rituximab | Ruxience PF-05280586 | Jul 2019 | Apr 2020 | MHRA | Sep 2019 | May 2020 | · | Feb 2021 | 6/7 |
| Trastuzumab | Trazimera PF-05280014 | Mar 2019 | Jul 2018 | MHRA | Sep 2018 | Aug 2019 | · | Apr 2020 | 6/7 |
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 Pfizer is the licence holder or applicant in one or more markets.
| Molecule | Brand | Market | Holder or applicant | Approved | Developer |
|---|---|---|---|---|---|
| Epoetin alfa and zeta | Retacrit | EMA | Pfizer Europe MA EEIG | Dec 2007 | Norbitec (Stada and Hospira) |
| Epoetin alfa and zeta | Retacrit | FDA | Hospira Inc., a Pfizer Company | May 2018 | Norbitec (Stada and Hospira) |
| Infliximab | Inflectra | EMA | Pfizer Europe MA EEIG | Sep 2013 | Celltrion |
| Infliximab | Pfizer (INN only) | CDSCO | Pfizer Limited | Sep 2021 | Celltrion |
In development
ClinicalTrials.gov lists four comparative trials sponsored by Pfizer for three molecules: bevacizumab, filgrastim, pegfilgrastim. All of these candidates already have at least one approval in the seven markets.
| Molecule | Candidate | Developer or sponsor | Reference product | Phase | Design | Registry status | Started | Primary completion | In the Atlas | Registry record |
|---|---|---|---|---|---|---|---|---|---|---|
| Bevacizumab | PF-06439535 | Pfizer | Avastin | Phase 1 | Comparative PK | Completed | Jan 2014 | Aug 2014 | Zirabev | NCT02031991 |
| Bevacizumab | PF-06439535 | Pfizer | Avastin (as licensed reference) | Phase 1 | Comparative PK | Withdrawn | Jan 2021 | Jul 2021 | Zirabev | NCT04126044 |
| Filgrastim | Filgrastim Hospira | Pfizer | Neupogen | Phase 1 | Comparative PK | Completed | Oct 2016 | Jan 2017 | Nivestym / Nivestim | NCT02923791 |
| Pegfilgrastim | PF-06881894 | Pfizer | Neulasta | Phase 1 | Comparative PK | Completed | Oct 2017 | Jul 2018 | Nyvepria | NCT03273842 |
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 Pfizer, by number of shared molecules. Overlap is the clearest sign of who competes with whom for the same tenders and licensing partners.
Chronology
- EMAJun 2010Nivestim, filgrastim
- FDADec 2017Ixifi, infliximab
- EMAMay 2018Zessly, infliximab
- PMDAJul 2018Infliximab BS [Pfizer], infliximab
- FDAJul 2018Nivestym, filgrastim
- EMAJul 2018Trazimera, trastuzumab
- PMDASep 2018Trastuzumab BS [Pfizer], trastuzumab
- EMAFeb 2019Zirabev, bevacizumab
- FDAMar 2019Trazimera, trastuzumab
- HCJun 2019Zirabev, bevacizumab
- PMDAJun 2019Bevacizumab BS [Pfizer], bevacizumab
- FDAJun 2019Zirabev, bevacizumab
- FDAJul 2019Ruxience, rituximab
- HCAug 2019Trazimera, trastuzumab
- PMDASep 2019Rituximab BS [Pfizer], rituximab
- FDANov 2019Abrilada, adalimumab
- EMAFeb 2020Amsparity, adalimumab
- EMAApr 2020Ruxience, rituximab
- EDEApr 2020Trazimera, trastuzumab
- HCApr 2020Nivestym, filgrastim
- HCMay 2020Ruxience, rituximab
- FDAJun 2020Nyvepria, pegfilgrastim
- HCOct 2020Nyvepria, pegfilgrastim
- EMANov 2020Nyvepria, pegfilgrastim
- EDEDec 2020Zirabev, bevacizumab
- HCJan 2021Abrilada, adalimumab
- EDEFeb 2021Ruxience, rituximab
- HCDec 2021Ixifi, infliximab
- EDEMay 2024Nyvepria, pegfilgrastim
Compare Pfizer 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