$ERNA

Ernexa Therapeutics (NASDAQ: ERNA) appointed Dr. Robert J. Spiegel to its board, leveraging his oncology expertise as it advances lead program ERNA-101 toward clinical trials. ERNA-101 showed complete tumor clearance and 100% survival in preclinical ovarian cancer studies. The company targets an IND submission in Q4 2026 and a first-in-human study in Q1 2027, aiming to treat platinum-resistant ovarian cancer and potentially other solid tumors.

Ernexa Therapeutics (ERNA) reported positive safety results from three IND-enabling studies of ERNA-101, its lead cell therapy. The studies showed no adverse findings, no teratoma formation, and no significant signal in non-tumor tissues. The company remains on track for a Q4 2026 IND submission.

Ernexa Therapeutics Inc. (ERNA) filed an SEC Form 8-K — Departure of Directors or Certain Officers; Election of Directors; Appointment of Certain Officers: Compensatory Arrangements of Certain Officers. Item 5.02 Departure of Directors or Certain Officers; Election of Directors; Appointment of Certain Officers; Compensatory Arrangements of Certain Officers. On September 14, 2026, upon the recommendation of the Nominating and Corporate Governance Committee of the board of directo

Ernexa Therapeutics (Nasdaq: ERNA) reported positive preclinical data for ERNA-201, showing disease-modifying activity in a rheumatoid arthritis model. The company will focus resources on advancing ERNA-101 for ovarian cancer, aiming for an IND submission by Q4 2026. ERNA-201's results validate the versatility of Ernexa's iMSC platform, which can be engineered for various diseases.

Ernexa Therapeutics said an independent study reproduced prior UT Anderson Cancer Center results for its ERNA-101 cell therapy, showing complete tumor clearance and durable long-term survival in a larger cohort. The company reported 10 of 15 animals (67%) cleared tumors with ERNA-101 plus anti-PD-1, while other groups had none. Ernexa targets an IND in Q3 2026 and a phase 1 trial in Q4 2026; shares rose 7.43% to $6.51.

Ernexa Therapeutics (Nasdaq: ERNA) said an independent CRO reproduced preclinical results for ERNA-101 plus anti-PD-1 in an ovarian cancer model. In 15 treated animals, 10 (67%) had complete tumor clearance and durable long-term survival, while no complete responses occurred in ERNA-101, anti-PD-1, or control arms. The company plans an IND in Q3 2026 and Phase 1 in Q4 2026.

Ernexa Therapeutics (NASDAQ:ERNA) shares rose 30% after independent preclinical validation of its lead cell therapy ERNA-101 in ovarian cancer models. According to the company, an independent CRO reproduced earlier results, with ERNA-101 plus anti-PD-1 achieving complete tumor clearance and long-term survival in 10 of 15 animals. The company plans an IND submission in Q3 2026 and Phase 1 in Q4 2026.

Ernexa Therapeutics Inc. (ERNA) filed an SEC Form 8-K — Submission of Matters to a Vote of Security Holders. EX-10.1 2 ex10-1.htm EX-10.1 Exhibit 10.1 ERNEXA THERAPEUTICS INC. 2026 OMNIBUS EQUITY INCENTIVE PLAN TABLE OF CONTENTS PAGE Article 1. Effective Date, Objectives and Duration 1 1.1 Effective Date of the Plan 1 1.2 Objectives of the Plan 1 1.3 Duration of the Plan 1 Article 2. De

Ernexa Therapeutics Inc. (ERNA) filed an SEC Form 8-K — Departure of Directors or Certain Officers; Election of Directors; Appointment of Certain Officers: Compensatory Arrangements of Certain Officers. false 0000748592 0000748592 2026-06-22 2026-06-22 iso4217:USD xbrli:shares iso4217:USD xbrli:shares 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 Repor

Ernexa Therapeutics (Nasdaq: ERNA) said manufacturing and IND-enabling work for its lead oncology candidate ERNA-101 is progressing. The company reported GMP production underway and expects an IND submission in Q3 2026, with a Phase 1 first-in-human study planned for Q4 2026. Ernexa also cited preclinical results with PD-1 blockade and completed a $10.5 million financing.