Clinical Trials

Verified stories whose regulatory record supports clinical-trial access. Eligibility and enrollment are never guaranteed.

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18 verified trial-access stories match your filters.

Important: Eligibility and enrollment are not guaranteed, and listing here is not a treatment recommendation. Talk to your care team.

Landmark NHS-Galleri multi-cancer blood-test trial missed its primary goal, but found real gains in earlier-stage detection

Regulatory status: InvestigationalEvidence stage: Later-Stage Human
Trial identifier
10.1200/JCO.2026.44.17_suppl.LBA100
View trial details
Study design
Randomized controlled trial
Population
Asymptomatic adults aged 50-77 in the United Kingdom, randomized to annual Galleri multi-cancer early detection (MCED) blood testing added to standard NHS cancer screening, or standard screening alone, followed for cancer diagnoses over multiple screening rounds.
Last reviewed
2026-08-13

Regulatory status by jurisdiction

Unspecified jurisdiction

Status
Investigational
Last verified
2026-08-13

This record has no structured cancer-type scope on file yet — editorial review recommended before treating it as applicable to a specific cancer type.

Primary evidence supporting this story

Eligibility varies — review trial criteria.

A widely-shared case series claiming a veterinary dewormer treats cancer was retracted — for an undisclosed conflict of interest, not disproven data

Regulatory status: InvestigationalEvidence stage: Early Human
Trial identifier
10.1159/000549387
View trial details
Study design
Case series / case report
Population
Three adult patients with stage IV cancers (breast, prostate, and melanoma) who self-administered fenbendazole, an over-the-counter veterinary dewormer with no FDA approval for any human use, alongside their own separately-received standard cancer treatment, as described in a since-retracted case series.
Last reviewed
2026-08-13

Regulatory status by jurisdiction

Unspecified jurisdiction

Status
Investigational
Last verified
2026-08-13

This record has no structured cancer-type scope on file yet — editorial review recommended before treating it as applicable to a specific cancer type.

Primary evidence supporting this story

Eligibility varies — review trial criteria.

Personalized mRNA cancer vaccine plus pembrolizumab reduces melanoma recurrence risk in randomized phase 2b trial

Regulatory status: InvestigationalEvidence stage: Emerging Clinical
Cancer type
Melanoma / Skin Cancer
Trial identifier
10.1016/S0140-6736(23)02268-7
View trial details
Study design
Randomized controlled trial
Population
Adults with resected, high-risk (stage IIIB-IV) melanoma, randomized 2:1 to individualized neoantigen therapy mRNA-4157/V940 plus pembrolizumab (107 patients) or pembrolizumab alone (50 patients), in the randomized, open-label, phase 2b KEYNOTE-942 trial.
Last reviewed
2026-08-13

Regulatory status by jurisdiction

Unspecified jurisdiction

Status
Investigational
Last verified
2026-08-13

This record has no structured cancer-type scope on file yet — editorial review recommended before treating it as applicable to a specific cancer type.

Primary evidence supporting this story

Eligibility varies — review trial criteria.

A lab-made “molecular glue” reprograms a lymphoma oncogene to trigger cancer-cell self-destruction, in early cell and mouse studies

Regulatory status: InvestigationalEvidence stage: Preclinical
Cancer type
Lymphoma
Trial identifier
10.1101/2025.03.14.643404
View trial details
Study design
Laboratory (preclinical)
Population
Laboratory cell-line panels (including 859 distinct cancer cell lines used to test selectivity) and mouse xenograft models of diffuse large B-cell lymphoma (DLBCL) — no human patients have been treated with this compound.
Last reviewed
2026-08-13

Regulatory status by jurisdiction

Unspecified jurisdiction

Status
Investigational
Last verified
2026-08-13

This record has no structured cancer-type scope on file yet — editorial review recommended before treating it as applicable to a specific cancer type.

Primary evidence supporting this story

Eligibility varies — review trial criteria.

Single glioblastoma case leads to Phase II test of neoadjuvant checkpoint immunotherapy

Regulatory status: InvestigationalEvidence stage: Early Human
Cancer type
Brain / CNS Cancer
Trial identifier
10.1038/s41591-025-03512-1
View trial details
Study design
Case series / case report
Population
One glioblastoma patient (case report); GIANT trial: newly diagnosed IDH-wildtype glioblastoma, estimated enrollment 92.
Last reviewed
2026-08-11

Regulatory status by jurisdiction

Unspecified jurisdiction

Status
Investigational
Last verified
2026-08-11

This record has no structured cancer-type scope on file yet — editorial review recommended before treating it as applicable to a specific cancer type.

Primary evidence supporting this story

Eligibility varies — review trial criteria.

AMBASSADOR trial finds adjuvant pembrolizumab extends disease-free survival in high-risk bladder cancer — not yet FDA-approved for this use

Regulatory status: InvestigationalEvidence stage: Later-Stage Human
Cancer type
Bladder Cancer
Trial identifier
10.1056/NEJMoa2401726
View trial details
Study design
Randomized controlled trial
Population
Adults with high-risk muscle-invasive or locally advanced urothelial (bladder) carcinoma, following radical surgical removal of the bladder (radical cystectomy or nephroureterectomy), randomized to adjuvant pembrolizumab or observation alone.
Last reviewed
2026-08-13

Regulatory status by jurisdiction

Unspecified jurisdiction

Status
Investigational
Last verified
2026-08-13

This record has no structured cancer-type scope on file yet — editorial review recommended before treating it as applicable to a specific cancer type.

Primary evidence supporting this story

Eligibility varies — review trial criteria.

BNT116 lung-cancer vaccine remains under study in first-in-human trial

Regulatory status: InvestigationalEvidence stage: Early Human
Cancer type
Lung Cancer
Trial identifier
NCT05142189
View trial details
Study design
Non-randomized trial
Population
NSCLC patients (exact eligibility/staging not specified by the frozen source).
Last reviewed
2026-08-11

Regulatory status by jurisdiction

Unspecified jurisdiction

Status
Investigational
Last verified
2026-08-11

This record has no structured cancer-type scope on file yet — editorial review recommended before treating it as applicable to a specific cancer type.

Primary evidence supporting this story

Eligibility varies — review trial criteria.

PT217, an investigational DLL3/CD47 bispecific antibody, remains under first-in-human study for neuroendocrine cancers

Regulatory status: InvestigationalEvidence stage: Early Human
Trial identifier
NCT05652686
View trial details
Study design
Non-randomized trial
Population
Adults with advanced, DLL3-expressing neuroendocrine carcinomas, including small cell lung cancer, large cell neuroendocrine carcinoma of the lung, and extrapulmonary neuroendocrine carcinoma (a category including neuroendocrine prostate cancer), enrolled in a first-in-human, open-label, dose-escalation/dose-expansion trial (SKYBRIDGE, NCT05652686). A reported target enrollment of approximately 203 patients was not independently confirmed against the trial registry itself in this research pass.
Last reviewed
2026-08-13

Regulatory status by jurisdiction

Unspecified jurisdiction

Status
Investigational
Last verified
2026-08-13

This record has no structured cancer-type scope on file yet — editorial review recommended before treating it as applicable to a specific cancer type.

Primary evidence supporting this story

Eligibility varies — review trial criteria.

CancerDiscoveries summarizes verified records in its database. Absence of a listing here does not establish that a treatment lacks regulatory authorization or access.