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Core trends in 2023 FDA drug approvals: Oncology, neurology and hematology dominate

By Brian Buntz | January 4, 2024

FDA logo2023 was a big year for hematology, neurology and oncology, with the medical specialties seeing the most FDA approvals. In terms of sponsors, Pfizer had the most approvals with six total, followed by UCB and Chiesi, each with three apiece.

When looking at commercial prospects, AstraZeneca’s respiratory syncytial virus antibody Beyfortus could be the biggest blockbuster from the 2023 cohort with expected peak sales of $1.9 billion. Alzheimer’s drug Leqembi could also be a major success, making up for the tepid demand for Aduhelm, which won conditional approval in 2021. While Aduhelm’s sales have sputtered, Leqembi could see peak revenue of $4.8 billion according to analysts.

Oncology continues to be a hot specialty with the most competition among the newly approved drugs, as the FDA continues to green light new entrants in crowded target classes such as PD-1 inhibitors.

In 2023, Pfizer received FDA approval for a half dozen drugs across a range of medical specialties, including zavegepant (Zavzpret), a CGRP receptor antagonist used for migraine. The company also scored full approval for nirmatrelvir, ritonavir (Paxlovid), a SARS-CoV-2 main protease inhibitor plus a CYP3A inhibitor used to treat mild-to-moderate COVID-19. Rounding out the approvals were ritlecitinib (Litfulo), a JAK3 inhibitor for alopecia areata; somatrogon (Ngenla), a human growth hormone analogue for growth hormone deficiency; elranatamab (Elrexfio), a BCMA × CD3 T-cell engager for multiple myeloma; and etrasimod (Velsipity), an S1P receptor modulator for ulcerative colitis.


Belgian pharma company UCB scored approvals for three new meds in 2023, including rozanolixizumab (Rystiggo), an FcRn-targeted monoclonal antibody for generalized myasthenia gravis patients who are acetylcholine receptor- or MuSK-antibody-positive; zilucoplan (Zilbrysq), a complement C5 inhibitor for acetylcholine receptor-positive generalized MG; and bimekizumab (Bimzelx), an IL-17A/F-targeted monoclonal antibody for plaque psoriasis.

Also scoring three approvals was the Italian pharma Chiesi, including velmanase alfa (Lamzede), a recombinant α-mannosidase for non-CNS manifestations of α-mannosidosis; pegungalsidase alfa (Elfabrio), a PEGylated recombinant α-galactosidase Α for Fabry disease; and birch triterpenes (Filsuvez), a treatment for epidermolysis bullosa.


Filed Under: Hematology, Neurological Disease, Oncology, Regulatory affairs
Tagged With: Chiesi, drug development, FDA approvals, hematology, neurology, oncology, Pfizer, UCB
 

About The Author

Brian Buntz

As the pharma and biotech editor at WTWH Media, Brian has almost two decades of experience in B2B media, with a focus on healthcare and technology. While he has long maintained a keen interest in AI, more recently Brian has made making data analysis a central focus, and is exploring tools ranging from NLP and clustering to predictive analytics.

Throughout his 18-year tenure, Brian has covered an array of life science topics, including clinical trials, medical devices, and drug discovery and development. Prior to WTWH, he held the title of content director at Informa, where he focused on topics such as connected devices, cybersecurity, AI and Industry 4.0. A dedicated decade at UBM saw Brian providing in-depth coverage of the medical device sector. Engage with Brian on LinkedIn or drop him an email at [email protected].

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