Kintor Pharmaceutical announced that China’s NMPA has approved clinical trials for GT90008 (PD-L1/TGF-β dual-targeting antibody) for the treatment of advanced solid tumours.
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By Bioblast Editor | Oct 21, 2021
Kintor Pharmaceutical announced that China’s NMPA has approved clinical trials for GT90008 (PD-L1/TGF-β dual-targeting antibody) for the treatment of advanced solid tumours.
By Bioblast Editor | Oct 21, 2021
The NSW State Government pledged $96 million towards a RNA pilot manufacturing facility, to be established in partnership with NSW universities. The facility is expected to house laboratories and pre-clinical trial spaces to enable early-stage RNA-based drug development.
By Bioblast Editor | Oct 21, 2021
Biocon Biologics announced that pharmacy benefit management company Express Scripts will list Semglee® (interchangeable biosimilar insulin glargine) as a preferred insulin brand on its National Preferred Formulary.
By Bioblast Editor | Oct 20, 2021
MorphoSys announced that the first patient has been dosed in its Ph II trials evaluating felzartamab for patients with Immunoglobulin A Nephropathy.
By Bioblast Editor | Oct 20, 2021
HepaRegeniX announced a new collaboration with the Netherlands Cancer Institute to investigate HRX-0233 (MKK4 inhibitor candidate) in preclinical in vivo models with Kirsten rat sarcoma virus (KRAS) mutant tumours.
By Naomi Pearce | Oct 19, 2021
Originally published in World Intellectual Property Review 3 2021
After surviving the Great Patent Cliff of 2011–2016, the pharma/biopharma industry finds itself in the Second Gre...
By Bioblast Editor | Oct 19, 2021
Opthea announced that the first clinical trial sites in the Asia-Pacific region are now open for patient enrolment in its Ph III trials of OPT-302 (VEGF-C/-D ‘trap’ inhibitor).
By Naomi Pearce | Oct 19, 2021
The evolution of jurisprudence in Australia can have far reaching implications for legal practitioners in every jurisdiction. Two recent Federal Court decisions have given Australia...
By Naomi Pearce | Oct 18, 2021
05 Oct 21 | EU | Celltrion announced that it has submitted a Marketing Authorisation Application to the EMA seeking approval of regdanvimab for the treatment of COVID-19 in adults w...
By Naomi Pearce | Oct 18, 2021
Date: 20 May 2021 / 18 October 2021Court: Federal Court of AustraliaJudge: Greenwood J
Background
Australian Patent 2012388708 (Patent) relates to a device and its use ...
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