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Source document· July 8, 2026

UPDATE: Endogenex Announces Full Enrollment of the ReCET Clinical Study

View original at globenewswire.com
UPDATE: Endogenex Announces Full Enrollment of the ReCET Clinical Study MINNEAPOLIS, July 08, 2026 (GLOBE NEWSWIRE) -- Endogenex, a clinical-stage medical device company dedicated to improving outcomes in individuals with type 2 diabetes (T2D), announced that the ReCET Clinical Study has reached full enrollment…
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  • Completing enrollment reflects the significant unmet need in type 2 diabetes and growing recognition that treatment approaches beyond pharmacotherapy can offer real value; the duodenum's role in metabolic regulation is well established and REGENT-1 feasibility data provided a strong scientific basis for the ReCET trial, which can now test the hypothesis at scale in a blinded, controlled design.

    60% confidence
  • Maintaining adequate blood glucose control remains a substantial challenge for many T2D patients despite multiple medications; full enrollment is an important step toward determining whether targeted restoration of duodenal function can produce durable, clinically meaningful improvements in glycemic control.

    60% confidence
  • Reaching full enrollment is a defining moment for Endogenex and patients with type 2 diabetes; even with GLP-1 receptor agonists and SGLT2 inhibitors, the disease often progresses because the gut has gone untreated, and with 350 patients enrolled across two countries the company is focused on generating randomized evidence to bring the therapy to patients.

    60% confidence
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Q4 2026 Biopharma Catalyst Cluster: Late-Stage Readouts and Regulatory Milestones
October 2026 brings a dense run of Phase 3 wins (ALOFT-IPF, RESTORE-3), new data presentations (Roche, Bayer, Lilly, Vertex, Galderma) and regulatory steps (FDA acceptance of Roche's vamikibart BLA, Scholar Rock's EMA resubmission). The next big catalyst is the ivonescimab FDA PDUFA date on 2026-11-14. Obesity combination studies (REDEFINE 4, TOGETHER-PsO) and the 2027 Maritime-1 completion point to more catalysts ahead. QAIAx's speculative AI-linked trial claims (the QIII pilot, targeted for 2027) are an unrelated micro-cap sideshow with weak evidence, and have little in common with the large-cap pipeline news.
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EPKINLY Regulatory-Clinical Success Cascade
High probability of expanded label indications, additional combination approvals, and competitive positioning strength in follicular lymphoma market. Predicts positive commercial uptake and potential accelerated review for related indications.
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ING Group
Both facts record the same metric (shares_outstanding) for ING Group at the identical observation date (2025-12-31). FACT A states 2,902,437,688 shares; FACT B states 2,902 million shares (2,902,000,000). The difference is 437,688 shares (~0.015%). This is a genuine value conflict, though the discrepancy appears to result from FACT B rounding to the nearest million while FACT A provides the precise count.
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UPDATE: Endogenex Announces Full Enrollment of the ReCET Clinical Study — Source | Via News | Via News