Drug Approval | March 25, 2022
USFDA approves Janssen’s injectable regimen for HIV
Cabenuva was co-developed as part of a collaboration with ViiV Healthcare and builds on Janssen's decades-long commitment to combatting HIV
Cabenuva was co-developed as part of a collaboration with ViiV Healthcare and builds on Janssen's decades-long commitment to combatting HIV
USFDA also approved complementary diagnostic imaging agent, Locametz, after radiolabeling with gallium-68 for the identification of PSMA-positive lesions
The drug is indicated for use in combination with other drugs
The investment will accelerate the overall Sarclisa development program
Nulibry is approved by the U.S. Food and Drug Administration (USFDA) to reduce the risk of mortality in patients with molybdenum cofactor deficiency (MoCD) Type A, an ultra-rare, life-threatening paediatric genetic disorder
According to statistics, the global inhalation drug market reached US $ 25 billion in 2020
The approval marks the first-and-only immunotherapy-based treatment for use before surgery for non-small cell lung cancer
Novel delivery of established growth and neurotrophic factors enables local, sustained release for greater efficacy
TruPharma has commenced commercial marketing of Sage's approved generic cartridge product
The sNDA was supported by the clinical results from cohort B of a single-arm, multi-center, pivotal study (RELIANCE study) on Carteyva in adult patients with relapsed or refractory B cell non-hodgkin lymphoma in China
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