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Oracle Runs

Oracle findings and outcome history for Study to Assess Neoadjuvant Durvalumab (D) and Platinum-Based Chemotherapy (CT), Followed by Either Surgery and Adjuvant D or CRT and Consolidation D, in Resectable or Borderline Resectable Stage IIB-IIIB NSCLC (MDT-BRIDGE) (NCT05925530).

Runs
4
Findings
4
Latest Run
Apr 6, 2026, 2:08 PM
Resolution Evidence
All Oracle Findings

Every stored oracle finding for this trial, including pending, dismissed, rejected, superseded, and accepted items.

YESAccepted85% confidenceGrok 4.20 (xAI)

Will the results be positive?

Interim analysis (ESMO 2025) of this exact Phase 2 trial reports primary endpoint resection rate 85.7% (high R0 94.4%, pCR 27.6%). Sources explicitly frame as 'impressive', 'encouraging safety', outcomes 'consistent with AEGEAN'. Primary endpoint clearly met with positive interpretation for this trial.

Found Apr 6, 2026, 2:08 PMOutcome date Oct 1, 2025, 12:00 AMReviewed Apr 6, 2026, 2:26 PM
NO_DECISIONDismissed90% confidencemanual-chat-review

Will the results be positive?

ClinicalTrials.gov still lists this study as active not recruiting with no posted results, so there is not yet a clear public positive or negative trial readout.

Found Apr 4, 2026, 8:54 PMReviewed Apr 4, 2026, 10:33 PM
NO_DECISIONDismissed88% confidenceGPT-5.4 (OpenAI)

Will the results be positive?

A public interim readout exists, but the cited trial-specific evidence is still ambiguous. The ESMO 2025 abstract reports promising interim numbers, yet does not clearly say MDT-BRIDGE met its primary endpoint or deliver a definitive positive/negative framing. AstraZeneca’s trial-summary page also says no results documents are posted yet.

Found Apr 3, 2026, 4:02 PMReviewed Apr 3, 2026, 4:47 PM
NO_DECISIONDismissed84% confidenceGPT-5.4 (OpenAI)

Will the results be positive?

Only an interim public readout was found. Non-official conference/commentary sources describe MDT-BRIDGE as encouraging/promising, but AstraZeneca’s trial-summary page shows no posted results document. Because the evidence is interim and incomplete rather than a clear final trial-specific sponsor readout, this is best classified as no_decision.

Found Apr 1, 2026, 6:35 PMReviewed Apr 1, 2026, 6:36 PM
Outcome History

Public history of accepted oracle reviews and recorded outcome changes for this trial.

Accepted Oracle ReviewApr 6, 2026, 2:26 PM

Will the results be positive?

PendingtoYEScurrentYES
Grok 4.20 (xAI)85% confidenceReviewed Apr 6, 2026, 2:26 PM

Interim analysis (ESMO 2025) of this exact Phase 2 trial reports primary endpoint resection rate 85.7% (high R0 94.4%, pCR 27.6%). Sources explicitly frame as 'impressive', 'encouraging safety', outcomes 'consistent with AEGEAN'. Primary endpoint clearly met with positive interpretation for this trial.