Chinese pharmaceutical company Simcere Pharmaceutical Group and a privately held, clinical-stage pharmaceutical company Aeromics Inc on Monday jointly reported a collaboration and exclusive license agreement for AER-271 to treat stroke and other indications in Greater China.
The companies added that AER-271 is a first-in-class, proprietary, intravenous (IV) prodrug that delivers AER-270, a potent inhibitor of AQP4 water channels for the treatment cerebral edema (brain swelling) in patients that have suffered ischemic strokes. AER-271 is an investigational drug that has successfully completed a Phase 1 study and is not yet approved by any regulatory agency.
Under the terms of the agreement, Simcere will be responsible for the clinical development and commercialisation of AER-271 in Greater China (mainland China, Hong Kong, Macau and Taiwan).
Pursuant to the partnership, Aeromics will receive an up-front payment and additional payments contingent on certain development, regulatory, and commercial milestones, plus tiered royalties on net sales ranging from high single digit to double digit percentages.
In conjunction with the agreement, Simcere will be responsible for leading development and commercialization of AER-271 in Greater China and will receive a single-digit percentage royalty from the net sales of AER-271 in the rest of the world.
Approximately 2,500,000 strokes are seen in China each year, many of which suffer life-threatening and severely disabling cerebral edema, or brain swelling and may benefit from an anti-edema medication.
Ascletis completes enrolment in Phase IIa US study of ASC30 for obesity
Antengene reveals ATG-022 clinical data at ESMO 2025
Sichuan Kelun-Biotech presents positive Phase 3 trial results for sac-TMT
SOPHiA DDM Digital Twins launched to simulate patient outcomes and support oncology decisions
Samsung to invest USD110m in GRAIL and commercialise cancer detection test Galleri in Asia
Jacobio Pharma partners with Oceanpine Capital to focus on core oncology pipeline
Viatris acquires Aculys Pharma including certain development and commercialisation rights
AstraZeneca expands Texas facility with USD445m investment to boost Lokelma production
Merck reports positive Phase 3 data for investigational two-drug HIV regimen doravirine/islatravir
Novocure announces presentation of new TTFields research at EANO and ESMO 2025 meetings
Minovia Therapeutics' MNV-201 receives FDA Orphan Drug Designation for Myelodysplastic Syndrome