Shares of Vanda Pharmaceuticals gained $2.53, or about 20%, on 31 January after the FDA approved the company’s drug Hetlioz (tasimelteon) as circadian regulator to treat non-24-Hour (non-24), a rare sleep-wake disorder, in patients with total blindness.
Shares of Vanda Pharmaceuticals gained $2.53, or about 20%, on 31 January after the FDA approved the company’s drug Hetlioz (tasimelteon) as circadian regulator to treat non-24-Hour (non-24), a rare sleep-wake disorder, in patients with total blindness.
Vanda's stock closed at $13.23 on 31 January, up 17 cents, or 1.3%.
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PolyPid's D-PLEX100 meets Phase III endpoints this time around, significantly reducing surgical point infections in abdominal colorectal surgery, and is set for a US approval submission early next year.
The company will ramp up manufacturing of its Jynneos vaccine to meet demand in worst-affected African countries and stockpiling richer nations.
2030 sales forecasts for Novo’s obesity hope are an order of magnitude larger than its closest rival among 2025’s expected debutantes.
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Pipelines in bioconjugates continue to develop, from ADCs to XDCs, with radionuclide drug conjugates (RDCs) and antibody-oligonucleotide conjugates (AOCs) leading the expansion.
Interim results from the Phase III REMARK study presented at WCLC showed the Chinese company’s second-generation ALK/ROS1 inhibitor met its primary endpoint as a first-line therapy in ALK-positive advanced NSCLC.
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