Neuland Laboratories Limited, a global contract development and manufacturing organization (CDMO) specializing in complex APIs, has entered into a development partnership with LIR Life Sciences Corp, a Canada‑based biotechnology company focused on scalable and accessible obesity treatments, to advance LIR Life’s cell‑penetrating peptide (CPP) platform.

As part of this engagement, Neuland will develop, test, and manufacture CPPs to support pharmacokinetic (PK) and pharmacodynamic (PD) studies, as well as Phase I formulations for LIR Life’s transdermal GLP‑1/GIP program.

Unlike traditional injectable formulations, LIR Life’s platform is designed to enable non-invasive administration, with the potential to improve patient adherence and broaden access. Currently, there are no approved transdermal GLP-1 therapies, positioning this approach as a potentially significant innovation in the treatment landscape.

For Neuland, the partnership highlights its expanding capabilities in peptide development and manufacturing, particularly in complex and emerging modalities such as CPP-enabled delivery systems. The company supports peptide programs from early development through commercial scale, with integrated capabilities spanning process development, scale-up, and cGMP manufacturing.

“We are excited to engage Neuland’s expertise in peptide development and manufacturing at both small and large scale,” said Edward Mills, CEO of LIR Life Sciences. “This partnership enables us to advance our CPP platform with the precision and consistency required for early-stage development.”

“This collaboration reflects the rapidly rising demand we see for CDMO’s that can advance complex peptide targets, particularly as new delivery technologies emerge” said Saharsh Davuluri, CEO of Neuland Laboratories. “LIR Life’s transdermal approach represents a novel application of GLP-1 therapies, and we look forward to supporting the development of their CPP platform through our integrated peptide capabilities.”