Palisade Bio (PALI) Piper Sandler 37th Annual Healthcare Conference summary
Event summary combining transcript, slides, and related documents.
Piper Sandler 37th Annual Healthcare Conference summary
6 Dec, 2025Key milestones and catalysts
Phase 1b cohort in fibrostenotic Crohn's disease to read out in early Q1 2025, with 6–12 patients.
IND filing for a definitive UC study planned for mid-2025, with final top-line readout expected by end of 2027.
Safety and toxicology data readouts expected in Q1 2025, supporting IND readiness.
Phase II UC study designed as a definitive, potentially registrational trial with 65 patients per arm and a 52-week blinded maintenance extension.
Recent $138 million fundraising ensures funding for Phase II studies in both UC and FSCD, with at least 1.5 years of runway post-study.
Scientific and clinical insights
Lead asset is a once-daily, oral prodrug PDE4 inhibitor targeting the terminal ileum and colon, activated by gut bacteria.
Demonstrated 100% clinical response and 40% clinical remission in a small UC cohort after one week, with rapid biomarker improvements.
Drug is 20 times more potent than Apremilast and designed to minimize adverse events by limiting upper gut absorption and Cmax.
Safety and tolerability are key differentiators versus other oral therapies, such as JAK inhibitors and S1Ps, which have black box warnings.
Mechanistically, the drug is both anti-inflammatory and antifibrotic, addressing high unmet needs in fibrostenotic Crohn's disease.
Study design and future plans
Phase II UC study will not use adaptive dose selection; all patients will be randomized to high, low, or placebo arms.
Key secondary endpoints include safety, tolerability, and efficacy across patient subgroups, including biologic-experienced and naive.
Phase 1b in fibrostenotic Crohn's will assess safety, PK/PD, histology, endoscopy, and ultrasound measures in symptomatic patients with ileal lesions.
Data from the Crohn's study will inform dosing for future UC studies.
Accelerated approval pathway for fibrostenotic Crohn's may use surrogate biomarkers and imaging endpoints, with post-marketing commitments.
Latest events from Palisade Bio
- PALI-2108 shows strong safety, efficacy, and precision targeting for IBD, advancing to Phase 2.PALI
Corporate presentation23 Mar 2026 - Strong cash position and positive clinical progress support advancement of IBD pipeline.PALI
Q4 202520 Mar 2026 - PALI-2108 shows promise as a safe, effective, once-daily oral IBD therapy with dual action.PALI
TD Cowen 46th Annual Health Care Conference3 Mar 2026 - Advancing a once-daily, gut-restricted PDE4 inhibitor with strong funding and pivotal trials ahead.PALI
Oppenheimer 36th Annual Healthcare Life Sciences Conference26 Feb 2026 - Advancing a locally-activated PDE4 inhibitor for UC, with phase I trials and pharma interest ahead.PALI
Virtual Investor Closing Bell Series3 Feb 2026 - Lead drug for ulcerative colitis targets higher remission rates with fewer side effects, entering trials soon.PALI
Virtual Investor Pitch Conference3 Feb 2026 - PALI-2108 demonstrates targeted efficacy and safety in IBD, with major market potential.PALI
Virtual Investor "Top 5 for '25"14 Jan 2026 - 8.9M shares registered for resale; lead IBD drug faces clinical and Nasdaq risks.PALI
Registration Filing16 Dec 2025 - Key votes include director elections, auditor ratification, and a reverse stock split for Nasdaq compliance.PALI
Proxy Filing2 Dec 2025