SATHGEN

THERAPEUTICS

State-of-the-art science for the hardest-to-treat cancers

We are seeking strategic partners for out-licensing, co-development and investment for our exciting lead molecule that has shown robust safety and efficacy against one of the most vicious of cancers - TNBC (triple negative breast cancer).
40+
Anti-Cancer Compounds
Phase Ia
Clinical Trials Complete
15+
Global Patents
2026
Phase II Target

Investment Highlights

Backed by established industrial conglomerates with a proven track record in healthcare and strong financial foundation for sustained growth.

Proven Market Potential

MSP008-22 has demonstrated compelling safety in Phase 1a trials with healthy volunteers and patients with solid tumors.

Robust IP Portfolio

Comprehensive global patent protection across multiple jurisdictions including USA, Europe, Japan, and emerging markets for sustained competitive advantage.

MSP008-22: Our Lead Asset

A first-in-class therapeutic with novel mechanism of action, currently in Phase I clinical trials with demonstrated efficacy across multiple cancer types and viral applications.

2023

Phase I Initiation - Advanced Solid Tumors

Initiation of phase I trials of MSP008-22 in patients with advanced solid tumors and healthy volunteers.

2024

First Cohort Completion

Completion of the dosing of the first cohort of patients in the phase I clinical trial of MSP008-22.

2025

Studies Completed

Completed studies in healthy volunteers and patients.

2026

Phase 1b/2

Clinical trials set to proceed onto phase 1b/2

Xenograft Studies

Xenograft studies with triple negative breast cancer cells show tumor growth inhibition upon single arm MSP008-22 or in combination with standard-of-care chemotherapy, Carboplatin.

Improved Efficacy

MSP008-22 improves the efficacy and lowers toxicity of another standard-of-care chemotherapy, Cisplatin, as shown by decreased IC50.

Safety Profile

MSP008-22 shows excellent safety profile in pre-clinical models including induced human blood lymphocytes.

Anti-Metastatic Efficacy

MSP008-22 also shows anti-stem cell and anti-metastatic efficacy in breast and prostate cancer models, in vitro.

SARS-CoV-2 Viral Load Reduction

Treatment with MSP008-22, both post-infection or prophylactic, reduces the SARS-CoV-2 viral load, and COVID-19-associated Pneumonitis, alveolar injury, and inflammation score.

Viral Replication Inhibition

MSP008-22 inhibits viral replication to the same extent as the anti-viral, Remdesivir.

Anti-SARS-CoV-2 Potential

MSP008-22 shows anti-SARS-CoV-2 potential as observed in cytopathic assays, comparable to Remdesivir.

Exceptional Investment Opportunity

Market-Leading Position

First-in-class mechanism targeting multiple high-value oncology indications with significant unmet medical need and market potential exceeding $10B globally.

De-Risked Investment

Strong preclinical data, active Phase I trials, comprehensive IP protection, and experienced management team with proven track record in drug development.

Global Expansion Ready

Established partnerships and regulatory pathways across major markets including US, Europe, and Asia-Pacific regions for rapid commercialization.

Key Metrics

Pipeline Value $500M+
Target Market Size $10B+
Patent Protection 2040+
Phase II Timeline 2026

Strategic Partnership Opportunities

We actively seek partnerships with pharmaceutical companies, research institutions, and investors to accelerate development and maximize global impact of our therapeutic programs.

Licensing Agreements

Regional or global licensing opportunities for MSP008-22 and pipeline compounds

Co-Development

Joint development programs with shared investment and risk mitigation strategies

Strategic Investment

Equity partnerships with pharmaceutical and biotech companies for mutual growth

Research Collaboration

Academic and industry partnerships for advancing novel therapeutic approaches

Connect With Our Team

Ready to discuss investment opportunities or strategic partnerships? Our experienced business development team is here to explore how we can work together.

Business Development

For partnership inquiries and investment opportunities

bd@sathgentherapeutics.com
+1 (732) 319-2091
103, Carnegie Center Dr, Suite 300, Princeton, NJ 08550, USA

A Strong Base

Sathgen Therapeutics has strong financial and technical support to help achieve its goals. Drug discovery and clinical trials are conducted at Sathgen division of Godavari Biorefineries Limited (GBL), and linked to the Somaiya Group, which is actively involved in healthcare and education.

Scroll to top