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Revolutionizing Crop Breeding: The Impact of Next-Gener...

A revolutionary shift is underway in the realm of agriculture as next-generation...

Advancements and Future Directions in Biomimetic Approa...

In the realm of modern chemistry and drug development, the innovative field of b...

Regeneron Shifts Strategy for Lymphoma Bispecific, Focu...

Regeneron has adjusted its regulatory approach for odronextamab, opting to pursu...

Teleflex Restructures Amidst €760 Million Biotronik Dea...

Teleflex has announced plans to restructure its operations by creating two indep...

Silence Therapeutics Halts Zerlasiran Phase 3 Despite 8...

Silence Therapeutics recently shared an update regarding its zerlasiran program,...

FDA Cancels Flu Vaccine Advisory Meeting, Raising Concerns

The Food and Drug Administration (FDA) has canceled its advisory panel meeting o...

New EU trial regulations could expedite approvals and a...

New EU Clinical Trial Regulations simplify international trials while offering t...

Inborn errors of metabolism elicit unique challenges fo...

As Rare Disease Day is commemorated on 28 February, experts discuss the barriers...

CHMP recommends AbbVie’s Rinvoq be approved for adult GCA

The CHMP has recommended the approval of AbbVie's upadacitinib (Rinvoq) for trea...

Rare disease treatments skipping UK patients largely du...

A survey has shown that pharma companies have low confidence their rare disease ...

Medigene and EpimAb to develop T cell engagers for soli...

Medigene and EpimAb Biotherapeutics have signed a co-development agreement invol...

Why pharma is still far from a treatment for galactosemia

With issues in therapy delivery and a barren trial landscape, short-term chances...

FDA accepts Sobi’s Gamifant application for HLH/MAS tre...

The FDA has accepted Sobi’s sBLA for Gamifant for haemophagocytic lymphohistiocy...

Exelixis focuses on future growth despite COSMIC-313 tr...

At the American Society of Clinical Oncology (ASCO) Genitourinary Cancer Symposi...

Alltrna plans to tackle rare diseases using tRNA-based ...

Alltrna’s CEO Michelle Warner said that the approach allows for basket trials th...

Zevra sells priority review voucher for $150m to suppor...

Zevra will use the $150m to support the commercial launches of rare disease drug...