Ascendiant Capital maintains Buy rating on Atossa Therapeutics, $25 price target

Atossa Therapeutics released an updated corporate presentation, highlighting progress in its (Z)-Endoxifen programs for oncology, MAS, and DMD. The company reported $26.1M in cash and no debt as of June 30, 2026, with funding expected to last into 2027. Key regulatory milestones and clinical updates were also provided, including Rare Pediatric Disease designations and planned Phase 2 trials for 2027.

Atossa Therapeutics (Nasdaq: ATOS) reported second-quarter 2026 results for the quarter ended June 30, 2026 and provided a corporate update. The company highlighted scientific updates for (Z)-endoxifen in rare pediatric diseases and ER+ breast cancer, including EVANGELINE Phase 2 progress. Atossa also completed a registered direct offering raising $4.5 million upfront, with potential gross proceeds up to $16.5 million.

ATOSSA THERAPEUTICS, INC. (ATOS) filed an SEC Form 8-K — Results of Operations and Financial Condition. Atossa Therapeutics Reports Second Quarter 2026 Financial Results and Provides a Corporate Update SEATTLE, WASHINGTON, August 7, 2026 — Atossa Therapeutics, Inc. (Nasdaq: ATOS) (Atossa or the Company), a clinical-stage biopharmaceutical company developing novel therapies in oncol

Tempus AI secured $192.5M in data agreements with BMS and Pathos AI. BMS will pay $137.5M for oncology data and software by 2031. Pathos may pay up to $55M for neurology data and tools, with payments tied to data delivery. Tempus restricted certain records from third-party licensing. According to the company's SEC filing.

IDEAYA Biosciences reported Phase 1 results for IDE849, showing antitumor activity in relapsed small cell lung cancer. Median overall survival was 17.4 months in second-line SCLC and 14.7 months across second-line and later-line patients. The confirmed response rate was 60.8% in second-line SCLC. IDEAYA plans Phase 3 trials. The stock closed at $36.12, up 1.83%, and is down 0.03% in premarket trading.

Pathos AI partnered with Bristol Myers Squibb and Tempus AI to develop AI tools for drug development in Alzheimer's and other neurological disorders. The company raised $237 million in a Series E funding round led by Bristol Myers, valuing it at $3 billion. Pathos will license data from Tempus for $55 million over five years and use its AI platform, Pathos Foundry, to study the dataset and design clinical trials. Bristol Myers gains non-exclusive access to Pathos Foundry.