
Monoclonal Antibody Developer

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Padcev, as the world's first ADC drug approved for the treatment of locally advanced or metastatic urothelial carcinoma (mUC), was initially approved in 2019, with sales reaching $450 million in 2022.
Interestingly, the day after Pfizer officially completed the acquisition of Seagen (December 25, 2023), the FDA approved Padcev in combination with K drug for first-line treatment of mUC, five months ahead of schedule.
Such a good omen in the post-epidemic eraPfizer Sees Arrival of "Next Growth Point"

Pfizer's Next Growth Point
In 2023, Pfizer's total annual revenue was $58.5 billion. Excluding the $12.5 billion contribution from COVID-19 products, traditional key products such as apixaban and the Prevnar series in areas like oncology, cardiovascular, and immunology remained the primary sources of income.
However, the sales of Pfizer's revenue pillars in the anti-tumor field—palbociclib (Ibrance), axitinib (Inlyta), and enzalutamide (Xtandi)—all declined year-over-year, and all three are small-molecule drugs.
Seagen's addition has greatly alleviated Pfizer's embarrassing situation of lacking "blockbuster tumor biologics."

At the 2024 Oncology R&D Day on February 29, Pfizer systematically outlined its future oncology strategy. The focus will be on four major common cancers: hematologic malignancies, breast cancer, urologic cancers, and thoracic cancers (including head and neck cancer); with an emphasis on three drug modalities: small molecules, ADCs, and bispecific antibodies.
The goal is to achieve by 2030,Increase the proportion of biologics to 65% (currently 5%), possess 8 key oncology drugs, and double the coverage of cancer patients.
Specifically, Pfizer's impact on Seagen's marketed productsActive Polishing(Expanded Indications), and forIts early pipelineOfContinuously Promote。
At present, this development strategy has begun to bear fruit.

First Glimpse of "Return": Seeking Approval for the Eighth Indication
On March 13, 2024, the phase 3 study ECHELON-3 of Adcetris in combination with lenalidomide + rituximab for the treatment of patients with relapsed/refractory diffuse large B-cell lymphoma (R/R DLBCL) achieved positive results.Compared with the active control group (placebo combined with lenaThalidomide + Rituximab) compared to,The primary endpoint OS was significantly improved, regardless of the CD30 response rate.
ECHELON-3 Study Aims to Explore Combination Regimens for Adcetris in Later-Line Treatment. Therefore, in terms of patient inclusion, patients must have received at least two prior lines of therapy, including relapse after CAR-T and stem cell transplantation.

Although Adcetris is approved for small cancer types, its market performance is acceptable.In 2023, the ADC drugs with sales exceeding Adcetris were only DS-8201 (approximately USD 2.7 billion) and T-DM1 (approximately USD 2.2 billion).
Currently, Pfizer plans to discuss the eighth indication for Adcetris with the FDA based on this trial data.
Except forAdcetris, inIn the field of hematological tumors, Pfizer currently hasMarketed products: BCMA/CD3 bispecific antibody Elrexfio (Erenatuzumab), Bosulif (Bosutinib);Products under research include the CD47 candidate drug Maplirpacept, the next-generation CD30 ADC (PF-08046044), and others.


“The Goose That Lays Golden Eggs”
$43 billion, Pfizer has bought the "goose that lays golden eggs."
Seagen's another key product, Padcev, after securing the world's first "PD-1 + ADC" combination therapy,Not only does this combined therapy demonstrate feasibility, but it also indicates broad application prospects.
Pfizer will further explore the application potential of the Padcev and K drug combination in cisplatin-tolerant and intolerant invasive bladder cancer, with relevant data expected to be released in 2026 and 2027.
Notably, Seagen's引进的荣昌生物HER2 ADC维迪西妥单抗is also undergoing a Phase III clinical trial in combination with K药for untreated HER2-positive bladder cancer patients.

In addition to the marketed products, many of Seagen's "assets under research" are also being actively advanced by Pfizer. This includes Seagen's integrin β-6-directed ADC drug Sigvotatug vedotin, which is currently in Phase 3 clinical trials for non-squamous non-small cell lung cancer populations.
Seagen's PD-L1 ADC PF-08046054 is currently in Phase 1 clinical trials for PD-L1 positive head and neck squamous cell carcinoma (HNSCC) population;
SGN-CEACAM5C, a CEACAM5 ADC co-developed by Seagen and Sanofi, is currently in Phase 1 clinical trials for various solid tumor populations...
After the $43 billion acquisition, Pfizer is steadily building up new growth points in the oncology field by deeply exploring Seagen's rich pipeline assets.
"ADC giant" is a positioning that Pfizer likes very much.
References:
1. Pfizer Official Website
2.clinicaltrials.gov
3. ADC at Pfizer Oncology R&D Day
4. Other Public Information

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