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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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  • 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
  • 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
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ESMO 2026 Oncology Data Wave Builds Toward Ivonescimab PDUFA, While Micro-Cap Biotech Exits the Market
Late October 2026 is a dense catalyst window led by ESMO 2026. Daiichi Sankyo's DXd antibody-drug conjugate (ADC) programs (DESTINY-Lung04, DESTINY-Breast11, REJOICE-Ovarian01/02, TUXEDO-3), Guardant's 25 abstracts and the PACE-LUNG ctDNA trial all report there. These feed into the FDA's 14 November 2026 PDUFA date for ivonescimab. Large and mid-cap developers with late-stage data and commercial launches (ZEGFROVY, ANKTIVA, MIUDELLA, lorundrostat, duvakitug) are drawing capital and attention. Spago Nanomedical's board decision to seek a Nasdaq First North delisting (EGM 19 November, application 25 January 2027) shows the capital squeeze on early-stage, single-asset names (Tumorad is Phase I).
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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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Ford Motor Company
Both facts give cash for Ford Motor Company at the same point in time (2025-12-31; FY 2025 year-end and Q4 2025 year-end are the same date). Both are labelled USD, but the values are 23,356,000,000 and 23.356, which cannot both be true in USD. The two numbers agree once the second is read as billions (23.356 bn = 23,356,000,000), so the economic content is consistent and the conflict is a unit/scale error in the Q4 2025 record. The period is not the reason for the conflict: a Q4 and an FY figure at the same year-end date should match.
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