Strategic Collaboration

Partnership opportunities & commercial models

Whether you're a pharmaceutical company looking to license a delivery platform or a hospital network seeking clinical validation, there's a defined model to engage with Miragen.

Two Partnership Tracks

Built for both ends of the pipeline

Pharmaceutical Companies

Co-development & technology licensing

  • Co-development programs — formulate existing oncology assets into BBB-penetrating nanotubes or injectable wafers
  • Combination therapies — develop synergistic regimens combining nanotherapeutics with standard-of-care agents
  • Technology transfer — full GMP scale-up transfer of lipid nanoparticle or polymer platforms
Hospital Networks

Clinical validation & trials

  • Clinical validation (SPR) — access to patient cohorts for validating biosensor sensitivity in breast and brain cancer
  • Post-surgical trials — collaboration with neurosurgery departments for injectable wafer efficacy studies
  • Early screening programs — deploy portable diagnostics for high-risk population screening initiatives
Engagement & Revenue Models

Five ways to structure a partnership

Indicative figures shown — final scope and pricing are agreed per project based on technology, territory, and exclusivity.

Consultancy

R&D Advisory

₹15–20L
per product
Development

Prototype Dev

₹63–71L
per therapeutic agent
Manufacturing

Scale-Up Services

₹30–40L
GMP facility, hands-on
Transfer

Tech Transfer

₹80–90L
full package transfer
IP Rights

Patent Licensing

₹10–85L
non-exclusive / exclusive
Regulatory Pathway

A defined route to market on both platforms

The SPR biosensor follows the CDSCO Class C (IVD) pathway under the Medical Devices Rules, 2017, with an estimated 18–24 months to market authorization. Nanotherapeutic platforms follow the New Drug pathway under NDCT Rules 2019, targeting accelerated approval routes, with an estimated 5–7 years to NDA.

Manufacturing follows Schedule M (GMP) and ISO 13485 standards, with adaptive trial designs and Orphan Drug Designation being pursued to reduce the GBM clinical timeline.

Join Our Mission

A three-step path to working together

01 · Review Data

Examine our preclinical dossiers and patent claims.

02 · Define Model

Select co-development, clinical trial, or licensing.

03 · Execute Pilot

Initiate a prototype study or validation trial.

Investment & Partnership Highlights

Why partner with Miragen

Evidence

Proven Science

10+ peer-reviewed publications validating BBB penetration and tumor suppression, with successful proof-of-concept in orthotopic models.

Protection

Strong IP Portfolio

2 granted Indian patents covering injectable wafers (No. 408307) and dermal delivery (No. 366070) form a robust defensive moat.

Relevance

Clinical Alignment

Directly addresses critical unmet needs in GBM survival (<7%) and affordable early cancer detection in India.

Breadth

Scalable Platforms

Versatile technologies spanning diagnostics, therapeutics, and cosmeceuticals create multiple revenue streams.

Let's Collaborate

Start the conversation with our team.