AZD7442 request for emergency use authorisation for COVID-19 prophylaxis filed in US

5 October 2021 - Filing includes data from PROVENT Phase 3 trial showing 77% reduction in risk of developing symptomatic COVID-19 ...

Read more →

The Product Monograph for Protopic has been updated

4 October 2021 - LEO Pharma Inc. today announced that Health Canada has approved an update to the Product Monograph of ...

Read more →

TGA grants provisional determination to Pfizer's COVID-19 treatment PF-07321332 and ritonavir

5 October 2021 - On 1 October 2021, the TGA granted provisional determination to Pfizer in relation to a new ...

Read more →

Heron Therapeutics announces filing of a supplemental new drug application for significant expansion of Zynrelef indication statement based on successful outcome of FDA type C meeting

4 October 2021 - FDA agreed to the immediate filing of supplemental new drug application to significantly expand the Zynrelef indication ...

Read more →

Comirnaty and Spikevax: EMA recommendations on extra doses and boosters

4 October 2021 - EMA’s CHMP has concluded that an extra dose of the COVID-19 vaccines Comirnaty (BioNTech/Pfizer) and Spikevax ...

Read more →

FDA’s naming rule for biosimilars has undermined Congress and health care

4 October 2021 - I recently tried to order white blood cell growth factor (pegfilgrastim) biosimilar for one of my ...

Read more →

Turning Point Therapeutics granted breakthrough therapy designation for repotrectinib treatment in patients with NTRK positive, TKI pretreated advanced solid tumours

4 October 2021 - Turning Point Therapeutics today announced the U.S. FDA granted a seventh regulatory designation to lead drug ...

Read more →

EMA receives application for marketing authorisation for Regkirona (regdanvimab) for treating patients with COVID-19

4 October 2021 - EMA has started evaluating an application for marketing authorisation for the monoclonal antibody Regkirona (regdanvimab, also known ...

Read more →

Pharmaceutical industry backs workplace vaccinations

5 October 2021 - Medicines Australia strongly recommends full COVID-19 vaccinations for the health and safety and protection of all ...

Read more →

ViiV Healthcare submits FDA application for first dispersible single tablet regimen containing dolutegravir for children living with HIV

4 October 2021 - ViiV Healthcare has announced it has made a regulatory submission to the U.S. FDA for approval of ...

Read more →

Enhertu granted breakthrough therapy designation in U.S.for patients with HER2 positive metastatic breast cancer treated with one or more prior anti-HER2 based regimens

4 October 2021 - Based on groundbreaking DESTINY-Breast03 results where Enhertu reduced the risk of disease progression or death by 72% ...

Read more →

Omeros provides regulatory update on biologics license application for narsoplimab in the treatment of hematopoietic stem cell transplant-associated thrombotic microangiopathy

1 October 2021 - Omeros Corporation today announced that the U.S. FDA notified the company that, as part of FDA’s on-going ...

Read more →

FDA, sponsors advance reliance on real world data & evidence

2 October 2021 - Demand for more efficient and faster development of medical products is prompting regulatory authorities to incorporate additional ...

Read more →

European Medicines Agency validates Bristol Myers Squibb’s application for LAG-3 blocking antibody relatlimab and nivolumab fixed dose combination as first-line treatment for patients with unresectable or metastatic melanoma

1 October 2021 - The Phase 2/3 RELATIVITY-047 trial served as the basis for this application, in which a statistically ...

Read more →

TGA advice on recognition of COVID-19 vaccines not registered in Australia but used internationally

1 October 2021 - The TGA has undertaken an assessment on the protection offered by certain COVID-19 vaccines that are ...

Read more →