Pharma News

Researchers from China found out in their recent study that use of Copper Intrauterine devices can be risky during pregnancy and it could compromise embryonic development.

Generally, IUDs (Intrauterine devices) are used to avoid pregnancy by women. But Women who use IUDs may become pregnant, albeit rarely, and many such women continue to use IUDs. Because it is difficult to remove or it may cause miscarriage.

The 7th Udai Pareek Memorial Oration was delivered virtually by Mr. Sanjiv Mehta, Chairman & MD, Hindustan Unilever Ltd. (HUL), on a current subject; of Organization and Leadership in a BANI World. The lecture was presided over by Padmavibhushan Dr. Raghunath Anant Mashelkar, National Research Professor and Chairman of the National Innovation Foundation.

Roche announced that Actemra/RoActemra (tocilizumab) intravenous (IV) has been granted World Health Organization (WHO) prequalification. Prequalification is a confirmation by WHO that Actemra/RoActemra meets the WHO standards for quality, safety and efficacy for the treatment of COVID-19 in adults who are receiving systemic corticosteroids and require supplemental oxygen or mechanical ventilation. It helps procurers in low- and middle-income countries identify priority medicines to improve access to care and support better health.

Quris, an artificial intelligence (AI) innovator disrupting the pharmaceutical arena, today announced it has signed an agreement with Merck KGaA, Darmstadt, Germany, a leading science and technology company, allowing Merck KGaA, Darmstadt, Germany to assess Quris’ BioAI safety prediction platform, comparing it to traditional in vitro and in vivo approaches.

The U.S. Food and Drug Administration (FDA) has accepted for Priority Review the supplemental Biologics License Application (sBLA) for Dupixent® (dupilumab) as an add-on maintenance treatment for children aged 6 months to 5 years with moderate-to-severe atopic dermatitis whose disease is not adequately controlled with topical prescription therapies or when those therapies are not advisable. The target action date for the FDA decision on this investigational use is June 9, 2022.

IIHMR University, Jaipur on Wednesday inaugurated its 26th Pradanya Annual Global Conference on Innovations in Healthcare and Education: The Decade of Acceleration for Global Goals, a 3-day conference attended by 30 speakers from 25+ country and over 2000 delegates. Dr. P.R. Sodani, President, IIHMR University welcomed the guest, speakers, and delegates in the inaugural session and introduced the conference theme and tracks to the audience. Dr.

Global pharma major Lupin Limited announced that it has received approval from the United States Food and Drug Administration (FDA) for its Abbreviated New Drug Application, Arformoterol Tartrate Inhalation Solution 15 mcg (base)/2 ml, Unit-dose Vials to market a generic equivalent of Brovana ® Inhalation Solution, 15 mcg /2 ml of Sunovion Pharmaceuticals Inc. (Sunovion).

Scientists at McMaster University who have developed an inhaled form of COVID vaccine have confirmed it can provide broad, long-lasting protection against the original strain of SARS-CoV-2 and variants of concern.

The research, recently published in the journal Cell, reveals the immune mechanisms and significant benefits of vaccines being delivered directly into the respiratory tract, rather than by traditional injection.

The phase II trial, led by researchers at St George’s, University of London and St George’s Hospital was joint-funded by the US-based Alzheimer’s Drug Discovery Foundation and the UK Alzheimer’s Society. The trial tested whether tadalafil increases brain blood flow in older men and women with narrowing of the brain arteries, a condition that can cause strokes and vascular dementia.