Staying abreast of the rapid changes in the healthcare environment is paramount. Through a combination of robust data, and expert opinion and analysis, we provide real-time actionable insights to our partners and enable them to make informed decisions.
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Cancer immunotherapy known to reactivate weakened immune cells of cancer patients, has yielded great success in recent years. Promising antitumor effects have been demonstrated in several solid and hematological malignancies by introducing PD-1/PDL-1 blockade therapy. There is a growing concern about whether they are comparable as the use of PD-1/PDL-1 inhibitors is increasing in number for the clinical treatment of cancer.
TEVIMBRA is a specially engineered humanized immunoglobulin G4 (IgG4) monoclonal antibody targeting programmed cell death protein 1 (PD-1) with high affinity and specificity. It is designed to reduce interaction with Fc-gamma (Fcγ) receptors on macrophages, enhancing the immune system’s ability to recognize and attack tumors.
Daiichi’s drug, TURALIO, is approved for adult TGCT patients experiencing severe morbidity or functional limitations for whom surgery is not a viable option. In its latest quarterly report for Q3 of the 2024 fiscal year, Daiichi reported a nearly 25% increase in TURALIO sales, reaching ¥5.1 billion (approximately $33.6 million).
The therapeutic paradigm for Polycythemia Vera patients has shifted significantly in the last few years. Previously, the Polycythemia Vera treatment landscape was dominated by generic medicines such as aspirin, hydroxyurea, interferons, and phlebotomy until the approval of JAKAFI (ruxolitinib) in the US in 2014,
Multiple system atrophy (MSA) is a rare and progressive neurodegenerative disorder that affects the autonomic nervous system, motor function, and balance. It manifests through a combination of parkinsonism, autonomic dysfunction, and cerebellar ataxia,
Merus had a standout start this month. Shortly after landing a long-anticipated commercialization partner for its zenocutuzumab, the drug has achieved FDA approval, becoming the first therapy to target cancers with a neuregulin 1 (NRG1) gene fusion.
On a global scale, Pompe disease affects approximately 2.0 cases per 100,000 live births, making it a rare yet significant condition. The late-onset form
A large client based in the USA wanted to in-license potential dMTS based drug delivery asset from companies involved in microneedle technology research for delivering therapeutic products.
A mid-sized pharma client was working to develop their asset portfolio and was interested in assessing best possible asset for atrial fibrillation for future development and licensing needs.
A medium pharmaceutical client with capabilities in novel formulations was involved in a deal with a manufacturing company for commercial-scale manufacturing of the client’s therapies.
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