Biopharmaceutical company company Halozyme Therapeutics Inc (Nasdaq: HALO) and biotechnology company Skye Bioscience Inc (Nasdaq: SKYE) announced on Monday that the companies entered into a non-exclusive global collaboration and licence agreement in December 2025 to evaluate nimacimab co-formulated with Halozyme's ENHANZE drug delivery technology for the treatment of obesity.
This agreement grants Skye rights to use ENHANZE to develop and potentially commercialise a higher-dose, subcutaneous formulation of nimacimab, enabling delivery of larger injection volumes. Skye will pay development and commercial milestones, while Halozyme will receive mid-single-digit royalties on net sales of ENHANZE-enabled nimacimab for at least 10 years.
Skye plans to initiate a Phase 2b obesity trial in mid-2026 to evaluate nimacimab with ENHANZE, including assessment in combination with a GLP-1 receptor agonist. Nimacimab is currently being studied in a Phase 2a obesity trial as a peripherally acting CB1 negative allosteric modulating antibody.
The collaboration expands Halozyme's ENHANZE platform, which supports subcutaneous delivery of biologics and is licensed to multiple global pharmaceutical partners, while advancing Skye's strategy to develop differentiated metabolic health therapies.
Relay Therapeutics wins FDA breakthrough status for zovegalisib in breast cancer treatment
DATROWAY receives US priority review for first-line metastatic triple negative breast cancer
Valneva and Instituto Butantan launch pilot chikungunya vaccination campaign in Brazil
Lupin launches Dasatinib tablets in US market
WuXi Biologics enters into licence and research service agreement with Vertex Pharmaceuticals
Natera submits Signatera CDx PMA to FDA for bladder cancer use
Pharming receives FDA complete response letter for paediatric Joenja application
Astrazeneca Imfinzi perioperative regimen gains positive EU CHMP opinion in early gastric cancer
I Peace generates human iPS cells from NKT cells and offers them for research use
Trace Biosciences' IND application for nerve-specific imaging agent approved by FDA
Frontage expands early phase clinical research capabilities across US and China
AstraZeneca agrees obesity and type 2 diabetes collaboration with CSPC
Ascletis Pharma Inc reports topline results from Phase III open-label study of denifanstat
Innovative Molecules GmbH completes Phase 1 clinical development programme for adibelivir
MicuRx Pharmaceuticals' IND application for MRX-5 cleared by FDA