$ELDN

Breakthrough T1D and Eledon Pharmaceuticals launched a clinical trial testing islet cell transplantation with tegoprubart in type 1 diabetes (T1D) patients with kidney disease. The trial includes 10 participants and is funded by an $8.5 million grant. Tegoprubart aims to reduce side effects compared to standard immunosuppressants, potentially benefiting a broader T1D population.

Eledon Pharmaceuticals (ELDN) submitted an IND application for Tegoprubart in islet cell transplants. Initial studies showed 12 patients achieved insulin independence. The company plans a Phase 3 kidney transplant trial in Q4 2026. ELDN stock closed at $2.99, up 2.34% in pre-market trading.

Eledon Pharmaceuticals, Inc. (ELDN) filed an SEC Form 8-K — Results of Operations and Financial Condition. Exhibit 99.1 Eledon Pharmaceuticals Reports Second Quarter 2026 Financial Results and Recent Business Highlights Successful End-of-Phase 2 meeting with FDA supports advancement of tegoprubart into a global Phase 3 kidney transplantation trial, on track to initiate in late 2026 Lo

Eledon Pharmaceuticals (NASDAQ:ELDN) reported a March 2026 balance sheet (May 2026) with $111m cash and no debt. The company’s cash burn was $69m over the prior year, implying about a 19-month runway. It recorded no revenue and cash burn rose 26%. Cash burn equals about 24% of its $289m market cap.

Analysts initiated coverage on several stocks. BMO Capital began coverage of Insmed (NASDAQ:INSM) with an Outperform rating and $192 target, and Axsome Therapeutics (NASDAQ:AXSM) with an Outperform rating and $310 target. Compass Point started American Healthcare REIT (NYSE:AHR) at Buy with $70 target. BMO initiated Trevi Therapeutics (NASDAQ:TRVI) at Outperform with $36 target, and Rodman & Renshaw started Eledon Pharmaceuticals (NASDAQ:ELDN) at Buy with $12 target.

NewcelX (Nasdaq: NCEL) said it completed a Type B Pre-IND meeting with the FDA for NCEL-101 in type 1 diabetes, with FDA feedback aligning on a regulatory path toward IND-enabling activities and a planned clinical trial. The trial would combine NCEL-101 with Eledon Pharmaceuticals’ (Nasdaq: ELDN) tegoprubart (anti-CD40L).

Eledon Pharmaceuticals, Inc. (ELDN) filed an SEC Form 8-K — Submission of Matters to a Vote of Security Holders. 8-K 0001404281 false --12-31 0001404281 2026-06-18 2026-06-18 UNITED STATES SECURITIES AND EXCHANGE COMMISSION WASHINGTON, D.C. 20549 FORM 8-K CURRENT REPORT Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934 Date of Report (Date of earliest event reported): J

Eledon Pharmaceuticals (ELDN) reported updated investigator-initiated trial results for tegoprubart, an anti-CD40L antibody, in type 1 diabetes patients receiving allogeneic islet cell transplants at the University of Chicago. According to the company, all 12 patients achieved insulin independence, with mean most recent HbA1c ~5.4% and stable graft function over a median 8 months (max 22). No rejection or de novo donor-specific HLA antibodies were reported. Eledon said it will seek FDA regulator

Eledon Pharmaceuticals Inc. (ELDN) has filed an SEC Form DEFA14A. The article also provides recent analyst ratings for ELDN, including targets from H.C. Wainwright, Guggenheim, Cantor Fitzgerald, and HC Wainwright & Co., alongside a list of related SEC filings and press releases concerning the company.

Data from Phase 2 BESTOW trial demonstrated a favorable safety and tolerability profile, substantially reducing the metabolic, neurologic, and cardiovascular toxicities commonly associated with tacrolimus