Medicenna Therapeutics (MDNA) 2026 Bloom Burton & Co. Healthcare Investor Conference summary
Event summary combining transcript, slides, and related documents.
2026 Bloom Burton & Co. Healthcare Investor Conference summary
21 Apr, 2026Program updates and clinical progress
MDNA11 is in phase I/II trials for solid tumors, showing 30–40% response rates as a single agent or with KEYTRUDA, with further data updates expected this year.
Proof of concept for MDNA11 will be demonstrated, with an FDA meeting planned by year-end to determine phase II registrational trial direction.
MDNA113, a first-in-class bispecific anti-PD-1, is set to enter clinical trials by year-end, with IND filing planned and recent preclinical data presented.
MDNA55 completed phase IIb with doubled median survival in recurrent glioblastoma; phase III trial is planned with a partner.
An Italian study is underway for MDNA11 in combination with nivolumab, aiming to delay surgery and prevent tumor recurrence in melanoma patients.
Scientific and competitive landscape
MDNA11 is an engineered IL-2 superagonist designed for safety, tumor targeting, and immune cell stimulation, differentiating it from previous IL-2 drugs.
Competitors have invested heavily in IL-2 programs with limited success; MDNA11’s unique approach is based on Stanford’s technology.
MDNA11 achieves tumor accumulation and response in patients who failed checkpoint inhibitors, with 30% response in second/third-line and 43% in combination with pembrolizumab.
Anti-PD-1 bispecifics are a major industry focus, with $38 billion in recent deals as KEYTRUDA and OPDIVO patents near expiry.
MDNA113 combines a potent, shielded IL-2 with anti-PD-1 and tumor targeting, aiming for superior efficacy and safety over competitors.
Preclinical data and safety profile
MDNA113 uses a masking domain and tumor-targeting ligand (IL-13Rα2) to localize and activate the drug at the tumor site, addressing aggressive cancers.
Preclinical studies show effective tumor accumulation, activation, and immune stimulation, with backup mechanisms for drug activation.
Head-to-head monkey studies show MDNA113 is much safer than competitor bispecifics, tolerating higher doses without severe toxicity.
MDNA113 demonstrates superior stimulation of CD8+ and gamma delta T cells compared to competitors, with less organ toxicity.
In rechallenge mouse models, cured animals did not develop tumors again, suggesting durable responses; a pancreatic cancer patient remains tumor-free months after stopping MDNA11.
Latest events from Medicenna Therapeutics
- MDNA11 and MDNA113 advance in clinical development, with cash runway into mid-2026.MDNA
Q2 202620 Apr 2026 - Lead immunotherapy assets deliver strong efficacy in resistant cancers, with major milestones ahead.MDNA
Corporate presentation23 Mar 2026 - Clinical and financial momentum continues, with expanded trials and improved net loss.MDNA
Q3 202613 Feb 2026 - MDNA11 demonstrates strong early efficacy and safety, with pivotal data expected in 2024–2025.MDNA
H.C. Wainwright 26th Annual Global Investment Conference 202420 Jan 2026 - All board nominees and the auditor were approved, with results to be published post-meeting.MDNA
AGM 202420 Jan 2026 - MDNA11 shows 30%-50% response rates in refractory cancers, with key data due by year-end.MDNA
Emerging Growth Conference 202517 Dec 2025 - MDNA11 delivers durable, well-tolerated responses and survival gains in refractory solid tumors.MDNA
KOL Event11 Dec 2025 - MDNA-11 demonstrates strong immune activation and durable responses in advanced solid tumors.MDNA
Oppenheimer 35th Annual Healthcare Life Sciences Conference (Virtual) 20253 Dec 2025 - Durable responses and pipeline progress highlight advances in engineered interleukin therapies.MDNA
Jones Healthcare and Technology Innovation Conference 202528 Nov 2025