The FDA grants accelerated approval to dostarlimab for rectal cancer, Lilly reports one-year remission data for pediatric ulcerative colitis, and Johnson & Johnson shares longer-term fistula remission results for Tremfya.
|Articles|June 15, 2002
- BioPharm International-06-01-2002
- Volume 15
- Issue 6
Criminal Penalties for Theft of Biological Material
Author(s)Liz Howard
by Liz Howard, Orrick, Herrington & Sutcliff, LLP Trade secret theft and economic espionage laws apply to biopharmaceutical researchers. Learn what your company needs to do to retain protection under the Economic Espionage Act and what employees need to know to pretect themselves from criminal charges.
Advertisement
Articles in this issue
over 24 years ago
Negotiating and Structuring Strategic Alliancesover 24 years ago
Finding Funding in Biotechnology: Keeping the Companies Aliveover 24 years ago
Stem Cells and Xenotransplantation: Ethics, Patents, and Politicsover 24 years ago
Unlocking the Value of R&D: Managing the Risksover 24 years ago
Viewpoint: United Kingdom highlights biomanufacturing capabilitiesover 24 years ago
Inside Washington: Safety, Risk, and Biotechnology RegulationAdvertisement
Related to this article
Accelerated approval for dostarlimab-gxly (Jemperli) pairs a single-arm phase 2 dataset with an FDA-authorized biomarker test and confirmatory requirements.
BMS's Dr Nathan Pennell outlines how biomarker testing barriers and trial diversity affect patient access to targeted oncology drugs.
In the phase 3 SHINE-2 trial, half of pediatric patients who responded to mirikizumab induction were in clinical remission at week 52. Lilly plans to file for a pediatric UC label expansion.
Guselkumab (Tremfya) sustained perianal fistula healing through 1 year in Crohn disease, with remission climbing to 35% in one FUZION dosing arm.
Roche will take ex-China development of Hansoh’s two preclinical ADCs and multiple programs against Roche-proposed targets once Hansoh completes global phase 1a trials. The deal includes $400 million upfront and more than $15 billion in potential milestones.
Cemiplimab's proposed EU regimen could cut Libtayo infusion visits from every 3 weeks to every 6 weeks, trimming infusion time by up to half.
Opus Genetics reports sustained vision gains with gene therapy, the FDA approves Roche’s Enspryng for at-home treatment of thyroid eye disease, and Estuary Biotherapeutics launches with $103 million to develop gene therapies for polycystic kidney disease.
Advertisement
Advertisement
Trending on BioPharm International
1
Roche, Hansoh Sign Second ADC Pact Covering Preclinical and Roche-Selected Targets
2
Regeneron's Libtayo Earns CHMP Nod for Expanded EU Dosing
3
Estuary Biotherapeutics Launches With $103 Million for ADPKD Gene Therapy
4
FDA Approves Roche’s Enspryng as First At-Home Subcutaneous Treatment for Thyroid Eye Disease
5