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The European Medicine Agency’s human medicines committee (CHMP) recommended marketing authorisations for the regulatory approval of three medicines at its January 2024 meeting last week. Additionally, a positive opinion for Niapelf (paliperidone), a genericmedicine for schizophrenia was adopted in the meeting.
These medicines were recommended by the CHMP to treat plaque psoriasis, paediatric plaque psoriasis, psoriatic arthritis, ulcerative colitis and Crohn’s disease. The post CHMP meeting highlights – July 2024 appeared first on European Pharmaceutical Review. Tuznue (trastuzumab) for breast and gastric cancer.
The first version of a list of critical medicines was published in 2023, with the aim to prevent disruption and help track EU manufacturing capacity and ensure the security of supply and availability of critical medicines at the EU level.
by the end of 2023 and may continue to rise in 2024 to 5%. Joy Polefrone, the executive director of the organization, says it aims to build a cluster of partners who are capable of manufacturing genericmedicines. JP Morgan predicts that the US unemployment rate could rise to 4.3%
The committee also recommended the biosimilar medicine Wezenla (ustekinumab) to treat of plaque psoriasis. Genericmedicine Eribulin Baxter (eribulin) was also granted a positive opinion by the committee, to treat breast cancer and liposarcoma. This covers paediatric plaque psoriasis, psoriatic arthritis and Crohn’s disease.
The gambit was prompted by the penalties that companies must pay to Medicaid when they raise the price of a medicine above the inflation rate, a consequence of a provision in a federal law that went into effect in early 2024. saying it will encourage innovation , The Financial Times notes. ” The U.S. government estimates.
Additionally, approval was recommended two genericmedicines: Enzalutamide Viatris (enzalutamide) to treat prostate cancer, and Nilotinib Accord (nilotinib) was also recommended to treat Philadelphia chromosome positive chronic myelogenous leukaemia.
At its February 2024 meeting, the EMA’s human medicines committee (CHMP) recommended the extension of marketing authorisations for six treatments, and positive opinions for the approval of ten medicines. These products were designated as an orphan medicine during their development.
percent between 2024 and 2031. Main drivers for the market were reported to be rising popularity of generics together with blockbuster and other small-molecule drugs going off-patent globally. Overall, increasing demand for genericmedicines will be a significant factor for growth. billion by 2031.
Is there a generic for Farxiga ? The pharmaceutical company Prasco currently markets a generic version of Farxiga. The generic is called dapagliflozin , which is the active ingredient in Farxiga. As of 2024, Prasco has offered an authorized generic version of dapagliflozin (more on authorized generics below).
Additionally, the CHMP recommended the genericmedicine Eltrombopag Accord (eltrombopag) to treat primary immune thrombocytopenia and thrombocytopenia associated with chronic hepatitis C. The EC questioned whether this would necessitate an update of the CHMPs opinion made in November 2024.
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