GlobeNewsWire
16 Jun 2026, 12:45 UTC · 1h ago
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Propanc Biopharma plans to submit a Phase 1b, First-In-Human (FIH) clinical trial application in Australia in 2026. — Advancing a lead asset into human trials is a critical value-inflection point for a clinical-stage biotech company.
+0.60The company has engaged a European CDMO to manage the pre-production, engineering run, and GMP manufacture of its lead asset, PRP. — Securing manufacturing partnerships reduces operational risk and confirms the transition from R&D to production readiness.
+0.30The Phase 1b study will target 30–40 advanced cancer patients with solid tumors using a novel combination of trypsinogen and chymotrypsinogen. — Defines the specific patient population and mechanism, though the small sample size limits immediate market impact.
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The company is making tangible progress toward its Phase 1b clinical trial by securing a CDMO partner and planning GMP production for its lead asset.
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