Find → Understand → Decide
Gemcitabine
Discovery priority: MEDIUM · POSSIBLE / INVESTIGATE
Discovery priority ≠ investment recommendation. These are observation labels, not verified canonical products. Buyer qualification: UNKNOWN.
Why investigate?
Why stranded (event context): inadequate public evidence; strategic reprioritization
Why now: Historical lead requires current reconfirmation; no fresh transaction catalyst established
Company/trial failed before biology? UNKNOWN
Biology implicated: UNCLEAR · Failure context: CORPORATE/FINANCIAL
MODEL INFERENCE · LOW confidence. Explicit asset-linked program event or documented experimental trial arm, stop scope, dated recency and biological cautions; no publication count or buyer-gate input.
Current control: UNKNOWN · Restart: UNKNOWN · Development reuse: UNKNOWN
Next diligence: Confirm present program status and exact product identity, then trace scoped rights/data/CMC and review arm-level human outcomes.
Existing buyer gates
Human Signal: UNKNOWN
Cheap Truth: UNKNOWN
Clean Rights: UNKNOWN
Market Pull: UNKNOWN
No event or publication count supplies missing gate evidence. Existing reviewed opportunities remain in their original records.
Evidence timeline
2015-06-23 · trial:NCT00624182
Registry update date, not proven program-stop date
SOURCE TEXT · Exact source
SUSPENDED
Trial reason is not attributed to every intervention; comparator/combination context needs review.
Interpretation: inadequate public evidence · AUTO_INFERRED · MEDIUM
Provenance and retrieval scope
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"type": "clinicaltrials",
"url": "https://clinicaltrials.gov/study/NCT00624182"
}2026-09-01 · trial:NCT05279300
Registry update date, not proven program-stop date
SOURCE TEXT · Exact source
The sponsor is temporarily pausing the trial to evaluate existing clinical data for long-term benefit-risk and optimize doses and dosing schedule.
Trial reason is not attributed to every intervention; comparator/combination context needs review.
Interpretation: inadequate public evidence · AUTO_INFERRED · MEDIUM
Provenance and retrieval scope
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"type": "clinicaltrials",
"url": "https://clinicaltrials.gov/study/NCT05279300"
}2026-09-04 · trial:NCT06050252
Registry update date, not proven program-stop date
SOURCE TEXT · Exact source
Other - evaluation of patients on first stage
Trial reason is not attributed to every intervention; comparator/combination context needs review.
Interpretation: inadequate public evidence · AUTO_INFERRED · MEDIUM
Provenance and retrieval scope
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"url": "https://clinicaltrials.gov/study/NCT06050252"
}2026-09-14 · trial:NCT04191135
Registry update date, not proven program-stop date
SOURCE TEXT · Exact source
Business Reasons
Trial reason is not attributed to every intervention; comparator/combination context needs review.
Interpretation: strategic reprioritization · AUTO_INFERRED · MEDIUM
Provenance and retrieval scope
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"type": "clinicaltrials",
"url": "https://clinicaltrials.gov/study/NCT04191135"
}2026-09-17 · trial:NCT00421096
Registry update date, not proven program-stop date
SOURCE TEXT · Exact source
Problems of recruitment
Trial reason is not attributed to every intervention; comparator/combination context needs review.
Interpretation: inadequate public evidence · AUTO_INFERRED · MEDIUM
Provenance and retrieval scope
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}Freshness is claim-specific
Fetching an old filing today does not establish current ownership or program status.
pipeline · PARTIAL · Not independently refreshed for current scoped claim · checked UNKNOWN
sec · PARTIAL · Not independently refreshed for current scoped claim · checked UNKNOWN
rights · PARTIAL · Not independently refreshed for current scoped claim · checked UNKNOWN
contact · PARTIAL · Not independently refreshed for current scoped claim · checked UNKNOWN
patent_assignment · PARTIAL · Not independently refreshed for current scoped claim · checked UNKNOWN
clinicaltrials · STALE · AREA[OverallStatus]TERMINATED AND AREA[StartDate]RANGE[2000-01-01,2014-12-31] AND (AREA[InterventionType]DRUG OR AREA[InterventionType]BIOLOGICAL) · checked 2026-09-21T21:43:00.118260+00:00
clinicaltrials · STALE · AREA[OverallStatus]TERMINATED AND AREA[StartDate]RANGE[2015-01-01,2026-09-21] AND (AREA[InterventionType]DRUG OR AREA[InterventionType]BIOLOGICAL) · checked 2026-09-21T21:43:00.930865+00:00
clinicaltrials · STALE · AREA[OverallStatus]SUSPENDED AND AREA[StartDate]RANGE[2000-01-01,2014-12-31] AND (AREA[InterventionType]DRUG OR AREA[InterventionType]BIOLOGICAL) · checked 2026-09-21T21:43:04.075140+00:00
clinicaltrials · STALE · AREA[OverallStatus]SUSPENDED AND AREA[StartDate]RANGE[2015-01-01,2026-09-21] AND (AREA[InterventionType]DRUG OR AREA[InterventionType]BIOLOGICAL) · checked 2026-09-21T21:43:05.182528+00:00
clinicaltrials · STALE · AREA[OverallStatus]SUSPENDED AND AREA[StartDate]RANGE[2015-01-01,2026-09-21] AND (AREA[InterventionType]DRUG OR AREA[InterventionType]BIOLOGICAL) · checked 2026-09-21T21:43:05.182528+00:00
Registry observations (6)
NCT00421096 · TERMINATED · PHASE2 · Uterine Cervical Cancer · Trial sponsor Centre Oscar Lambret
Reported aliases: None. Identity, treatment role and exposure require review.
NCT04191135 · TERMINATED · PHASE2 · Triple Negative Breast Neoplasms · Trial sponsor Merck Sharp & Dohme LLC
Reported aliases: GEMZAR®. Identity, treatment role and exposure require review.
NCT00624182 · SUSPENDED · PHASE1 · Bile Duct Cancer · Trial sponsor Akita University Hospital
Reported aliases: None. Identity, treatment role and exposure require review.
NCT06050252 · SUSPENDED · PHASE2 · Resectable Intrahepatic Cholangiocarcinoma · Trial sponsor National Cancer Institute (NCI)
Reported aliases: dFdC; dFdCyd; Difluorodeoxycytidine. Identity, treatment role and exposure require review.
NCT05279300 · SUSPENDED · PHASE1 · Advanced Solid Tumor; Advanced Lymphoma · Trial sponsor CStone Pharmaceuticals
Reported aliases: None. Identity, treatment role and exposure require review.
NCT01352962 · COMPLETED · PHASE1 · Urethral Neoplasms; Neoplasms, Urethral; Cancer of the Urethra; Urethral Cancer · Trial sponsor National Cancer Institute (NCI)
Reported aliases: None. Identity, treatment role and exposure require review.