Armata Pharmaceuticals, Inc. (ARMP) Reports Q3 Loss, Misses Revenue Estimates

Armata Pharmaceuticals (NYSE American: ARMP) reported Q2 2026 results for the quarter ended June 30, 2026, with $2.5M grant and award revenue, R&D of about $7.6M, G&A of about $5.2M, and an operating loss of about $10.3M. The company said it submitted the Phase 3 protocol for AP-SA02 to the FDA, received Fast Track and an agreed pediatric study plan, and received an additional $2.5M non-dilutive DoD funding.

Armata Pharmaceuticals, Inc. (ARMP) filed an SEC Form 8-K — Results of Operations and Financial Condition. EX-99.1 2 armp-20260812xex99d1.htm EX-99.1 Exhibit 99.1 ​ Armata Pharmaceuticals Announces Financial Results for the Second Quarter 2026 and Provides a Corporate Update ​ LOS ANGELES, Calif., August 12, 2026 - Armata Pharmaceuticals, Inc. (NYSE American: ARMP) (“Armata” or the “C

Armata Pharmaceuticals said it submitted the complete Phase 3 protocol for its AP-SA02 multi-phage therapy to the FDA, addressing End-of-Phase 2 feedback, and completed four engineering runs at its Los Angeles cGMP facility. The Phase 3 superiority study is planned to start in 2H 2026. The company received a $2.5M DoD continuation award. ARMP shares were up 10.27% to $4.97.

Armata Pharmaceuticals (ARMP) said the U.S. FDA agreed to its Initial Pediatric Study Plan for AP-SA02 in pediatric complicated Staphylococcus aureus bacteremia. The iPSP sets a framework to defer pediatric work until adult Phase 3 data, expected to start in H2 2026, then run a single multicenter open-label pediatric trial. ARMP shares closed July 10 at $4.26.

Johnson & Johnson (JNJ) proposed a $5.5B settlement for 76,000 talc-related lawsuits, but it requires 95% claimant approval and may exceed this amount. The company has $21B in cash and expects to pay $3B in 2027, with further payments starting in 2028. A judge's recent ruling may strengthen JNJ's legal position. Investors weigh the benefit of reduced uncertainty against potential higher costs.

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