Pearce IP provides weekly reports on global biosimilars activities in the Pearce IP BioBlast®. Significant biosimilar activities for the week ending 18 July 2025 are set out below:...
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Stay informed about important legal and industry news with our blogs and weekly BioBlast® updates.
By Naomi Pearce, Chantal Savage | Jul 22, 2025
Pearce IP provides weekly reports on global biosimilars activities in the Pearce IP BioBlast®. Significant biosimilar activities for the week ending 18 July 2025 are set out below:...
By Bioblast Editor | Jul 22, 2025
On 22 July 2025, Replimune announced that the FDA has advised it is unable to approve, in its present form, the Biologics License Application (BLA) for RP1 (vusolimogene oderparepvec) in combination with BMS’ Opdivo® (nivolumab) for the treatment of advanced melanoma. The ...
By Bioblast Editor | Jul 21, 2025
With a number of biosimilars to MSD’s Keytruda® (pembrolizumab) currently in clinical trials, we provide the following update on those trials and their status, based on previous reports and the information available to date in the clinicaltrials.gov registry:
Samsu...
By Bioblast Editor | Jul 21, 2025
On 21 July 2025, Samsung Bioepis published its US Biosimilar Market Report, which has been released every quarter since April 2023. The report details average sales price (ASP) and wholesale acquisition cost (WAC) information for commercially available biosimilars in the U...
By Bioblast Editor | Jul 18, 2025
On 18 July 2025, the Delhi High Court issued a preliminary injunction restraining Zydus Lifesciences from launching its nivolumab biosimilar (ZRC-3276) in India. The injunction was granted in proceedings brought by BMS alleging Zydus’ Indian launch of its nivolumab biosimi...
By Bioblast Editor | Jul 18, 2025
In an article dated 18 July 2025, HiT News reported on a hearing in a patent infringement lawsuit filed by Regeneron and Bayer against Sam Chun Dang (SCD) and Optus Pharmaceutical in the Seoul Central District Court. The lawsuit was filed by Regeneron/Bayer in January 2024...
By Paul Johns, Sally Paterson | Jul 18, 2025
The New Zealand government has reiterated its plans to reform the law and allow the advertisement at medical conferences and trade shows of medicines not approved by the New Zealand...
By Bioblast Editor | Jul 17, 2025
On 17 July 2025, Samsung Bioepis announced that it has entered into a licence, development and commercialisation agreement with eyecare pharmaceutical company, Harrow, in relation to Samsung Bioepis’ US ophthalmology portfolio. The agreement follows Biogen’s October 2024 d...
By Bioblast Editor | Jul 16, 2025
On 16 July 2025, Celltrion announced the results of its global phase 3 trial comparing the efficacy and safety of its tocilizumab biosimilar, Avtozma® (CT-P47), to reference drug, Roche’s Actemra®. The results demonstrated comparable efficacy, pharmacokinetics, safety and ...
By Bioblast Editor | Jul 16, 2025
On 16 July 2025, Bio-Thera Solutions announced that the FDA has accepted for review its Biological Licence Application (BLA) for BAT2506, biosimilar to J&J’s Simponi® (golimumab). BAT2506 is being developed and manufactured by Bio-Thera and will be commercialised in th...
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