Allarity Therapeutics Completes Additional Private Equity Financing

Allarity Therapeutics, Inc. (ALLR) filed an SEC Form 8-K — Results of Operations and Financial Condition. EX-99.1 2 ea030215701ex99-1.htm PRESS RELEASE, DATED JUNE 30, 2026 Exhibit 99.1 Allarity Therapeutics Reports Second Quarter 2026 Results and Completion of the Phase 3-Ready Stenoparib Manufacturing Campaign - Completed quarter with $26.9 million in cash and restricted cash - Key

Allarity Therapeutics (NASDAQ: ALLR) reported Q2 2026 results and said it ended June 30 with $26.9 million in cash and restricted cash. The company said the USPTO granted a key patent for its stenoparib-specific DRP companion diagnostic through April 2042, and it completed its stenoparib Phase 3-ready manufacturing campaign and obtained CLIA certification for in-house DRP testing.

Allarity Therapeutics (NASDAQ: ALLR) said it obtained CLIA Certificate of Registration for its in-house laboratory in Horsholm, Denmark, enabling it to run DRP® biomarker testing internally for FDA registration-related studies. The company expects faster turnaround, streamlined trial communication, and lower long-term costs, and may offer CLIA-compliant testing services to partners.

Shareholder Doug Bond filed a class action against UWM Holdings in Michigan federal court, alleging securities fraud over disclosures about UWM’s interest rate derivatives hedge tied to its Two Harbors acquisition. The suit covers purchases from March 9 to Aug. 5, citing a $603.2 million derivatives loss and a $2.05 billion Oaktree cash infusion after a March revenue projection.

The Pentagon signed seven-year framework agreements with Boeing and RTX to expand production of Standard Missile-3 components for SM-3 Block IB and Block IIA, including avionics and ejector assemblies Boeing supplies to Raytheon. The deals aim to stabilize supply chains and expand munitions output. Separately, the Missile Defense Agency awarded Raytheon a $745 million contract for Block IIA interceptors.

BrainStorm Cell Therapeutics (OTCQB: BCLI) reported Q2 2026 results for the quarter ended June 30, 2026. It said it is preparing to start the Phase 3b ENDURANCE study of NurOwn in ALS under an FDA-agreed Special Protocol Assessment, planning about 200 patients. Cash was about $0.2M vs $1.03M a year earlier, with Q2 net loss about $3.9M. The company appointed Peter J. Pitts as Executive Chairman and raised about $400k in private placements.