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- Korsana's Alzheimer’s antibody launches with $175M & Novartis signs a $1.7B deal with Unnatural Products
Korsana's Alzheimer’s antibody launches with $175M & Novartis signs a $1.7B deal with Unnatural Products

Good morning!
Going public before your first in-house hire? Bold move, but preclinical eye disease biotech EIR Biopharma is taking it anyway. The company has filed to raise up to $17.1M in an upcoming NYSE IPO.
Why it matters: The company’s lead candidate, EIR-1003, is a peptidomimetic targeting the Ephrin receptor to promote optic nerve regeneration, with plans to move into phase 1/1b in 2027 for indications including glaucoma, diabetic retinopathy and uveal melanoma. A second program, EIR-0205, is a cyclodextrin licensed from Cornell for dry age-related macular degeneration.
Yes, but: EIR is “semi-virtual,” run by two part-time executives, with preclinical work conducted at the University of Miami and Cornell.
Bottom line: The IPO window is open wide enough that, for some companies, the public markets are starting to look like the new seed round.
— Joachim E.
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SNAPSHOT
Korsana launches with $175M to test next-gen Alzheimer’s antibody in 2027
Boston-area startup Korsana Biosciences has emerged from stealth with $175 million to advance KRSA-028, an anti-amyloid antibody engineered to cross the blood-brain barrier, into the clinic by early 2027.
Why it matters: Alzheimer’s remains a massive unmet need, and current amyloid drugs carry safety risks and cumbersome IV dosing. Korsana aims to improve brain delivery, reduce anemia and brain swelling risks, and replace IV dosing with simple subcutaneous injections.
Backstory: Founded in 2024, Korsana raised a $25 million seed round and a $150 million series A led by Wellington Management and TCGX, with backing from J.P. Morgan Life Sciences Private Capital, Sanofi Ventures and Foresite Capital. CEO Jonathan Violin previously led Viridian, Dianthus and Quellis. KRSA-028 was discovered with Paragon Therapeutics.
Big picture: Korsana joins a crowded field of second-generation amyloid players trying to solve limitations of first-wave drugs like Leqembi, Kisunla and Aduhelm, particularly amyloid-related imaging abnormalities (ARIA) and delivery challenges. Roche, AbbVie (via Aliada), and Denali are pursuing similar transferrin receptor-based strategies.
Zoom in: KRSA-028 works by binding to transferrin receptors to shuttle across the blood-brain barrier and target amyloid beta. Korsana reduced the antibody’s effector function to avoid attacking young red blood cells, aiming to limit anemia while maintaining plaque clearance. Competition like Roche’s trontinemab is already in phase 3 but binds to reticulocytes as well as transferrin receptors, which might explain the 10%–20% anemia rates that have been observed.
What’s next: Korsana continues to collaborate with Paragon and is scouting external assets, with ambitions to build and independently scale a long-term neurodegeneration-focused biotech. The company plans to file for clinical entry in early 2027 and is expecting initial safety data by mid-2027, with proof-of-concept plaque reduction by year-end.
SNIPPETS
What’s happening in biotech today?
🤝 Unnatural deal: Novartis has entered a cardiovascular disease research and licensing deal with California-based biotech Unnatural Products (UNP) worth up to $1.8 billion, including $100 million in upfront and preclinical milestone payments. The agreement grants Novartis access to UNP’s AI-guided platform for developing orally and injectable macrocyclic therapeutics targeting historically “undruggable” proteins. Novartis will oversee IND-enabling studies, clinical development, manufacturing, and commercialization, while UNP is eligible for development, regulatory, and commercial milestones plus tiered royalties. The partnership builds on UNP’s previous deals with Merck and argenx, further validating its macrocyclic drug discovery platform.
🍀 Second chance: Eli Lilly is paying CSL $100 million upfront for rights to develop clazakizumab, an anti-IL-6 monoclonal antibody that previously failed in a phase 3 trial for chronic antibody-mediated rejection (AMR) in kidney transplant patients, which was terminated early for lack of efficacy. CSL will continue advancing clazakizumab in a separate phase 3 trial aimed at preventing cardiovascular events in patients with end-stage kidney disease on dialysis, expected to conclude in 2029. Under the agreement, CSL is also eligible for undisclosed milestones and royalties, while Lilly can pursue the therapy in additional indications.
🔄 Pipeline pivot: Sensei Biotherapeutics has avoided a potential shutdown by merging with privately held Faeth Therapeutics in an all-stock deal that gives Faeth shareholders 40.8% of the combined company and investors in a concurrent $200 million private placement a 54.3% stake, leaving existing Sensei shareholders with 4.9%. The merger adds Faeth’s phase 2-stage lead candidate PIKTOR, an oral combination targeting the PI3K/AKT/mTOR pathway, as the new focus, with upcoming phase 2 data in advanced endometrial cancer and a planned phase 1b trial in breast cancer. The financing extends runway through key readouts and marks a turnaround for Sensei, which had recently downsized amid dwindling cash.
💉 Flu filing: The FDA has accepted Moderna’s revised biologics license application for its mRNA flu vaccine, mRNA-1010, just days after issuing a refusal-to-file letter over concerns that the original trial comparator did not reflect the U.S. standard of care for seniors. Following discussions with the agency, Moderna amended its submission to seek full approval for adults ages 50 to 64 and accelerated approval for those 65 and older, with a post-marketing study commitment for the senior group. A decision is due by Aug. 5, positioning the company for potential launch ahead of the 2026–27 flu season and supporting its goal of reaching break-even by 2028.
🦠 Gut guard: PLL Therapeutics has reported positive phase I/II data for its investigational ALS therapy PL001, demonstrating safety and tolerability in a double-blind, placebo-controlled trial of 12 patients receiving subcutaneous doses, with no serious or treatment-related adverse events leading to discontinuation. PL001 uses a poly-L-lysine-based delivery platform to transport small-chain fatty acids aimed at restoring gut barrier integrity, based on research linking ALS to increased gut permeability and systemic inflammation. The company plans to advance to a 140-patient phase II trial in Australia and New Zealand to assess organ targeting, inflammation, and gut restoration.
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