RedHill Biopharma
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RedHill Biopharma (RDHL) investor relations material

RedHill Biopharma H1 2026 earnings summary

Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.
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H1 2026 earnings summary30 Sep, 2026

Executive summary

  • Strategic portfolio reset added exclusive commercialization rights to Rebyota and Clenpiq for $12M upfront, funded by the $18M upfront Talicia divestment proceeds.

  • Rebyota and Clenpiq generated a combined $37.5M in 2025 net sales under Ferring; the portfolio is supported by an established U.S. GI commercial infrastructure.

  • H1 2026 priorities included transitioning the two products and advancing oncology, Crohn’s disease, Ebola and other GI development programs.

Financial highlights

  • Continuing-operations revenue was $0 in H1 2026 vs. $0.3M in H1 2025, generated from the RHB-102 license agreement.

  • Operating loss was $4.1M vs. $3.4M; net loss was $6.1M vs. $4.1M in H1 2025.

  • Net financial expense was $1.6M vs. $0.5M net financial income in H1 2025, mainly reflecting warrant issuance costs and derivative fair-value adjustments.

Outlook and guidance

  • Priorities for H2 2026 and beyond include smooth product transitions, commercial growth, further complementary product additions and continued R&D progress.

  • Opaganib remains in a Bayer-supported Phase 2 prostate cancer study; recruitment continues, while the RHB-204 Crohn’s program is Phase 2-ready.

  • RHB-102 development includes GI intolerance associated with GLP-1/GIP therapies; a Phase 2-ready proof-of-concept study is planned.

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