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Luciann Nguyen
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NCT07450859phase 2recruiting

A Study of Nuzefatide Pevedotin (BT5528) in Patients With Metastatic Pancreatic Ductal Adenocarcinoma (PDAC)

BicycleTx Limited

ClinicalTrials.gov
39
Enrollment · estimated
1
Countries · 6 sites
2029-03
Primary completion
27 days ago
Record updated
Commercial relevance

No explicit biomarker / molecular-testing language identified in the public record.

Biomarker requirement language
  • Histologically confirmed metastatic pancreatic ductal adenocarcinoma (PDAC).
  • Participants must have failed whose disease has progressed on or after only 1 prior line of therapy or on or after second line therapy with a KRAS inhibitor, with evidence of radiographic progression. Neoadjuvant or adjuvant systemic therap
  • Participants must have sufficient tumor tissue (fresh or archived) available for analysis of EphA2 tumor expression and other biomarkers.
  • Known microsatellite instability-high (MSI-H) status and are eligible for immune checkpoint inhibitor therapy
Change timeline

No changes detected yet. The first refresh records a baseline snapshot; subsequent refreshes generate field-level changes.

Signals from this trial
  • New trial
    42/100
    Opportunity

    New phase 2 trial NCT07450859 posted by BicycleTx Limited: "A Study of Nuzefatide Pevedotin (BT5528) in Patients With Metastatic Pancreatic Ductal Adenocarcinoma (PDAC)".

    ClinicalTrials.gov record updated 26 days ago.

Eligibility — raw, for validation
Inclusion Criteria

* At least 18 years of age at the time of signature of the informed consent form (or at least 19 years where locally defined as minimum age of consent).
* Measurable disease as defined by RECIST v1.1.
* Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1.
* Life expectancy of at least 12 weeks.
* Histologically confirmed metastatic pancreatic ductal adenocarcinoma (PDAC).
* Participants must have failed whose disease has progressed on or after only 1 prior line of therapy or on or after second line therapy with a KRAS inhibitor, with evidence of radiographic progression. Neoadjuvant or adjuvant systemic therapy may count as the first line if the participant progressed less than 6 months from the end of systemic therapy. Prior treatment with KRAS inhibitors in the first-line setting is permitted if there was no intervening treatment prior to enrollment.
* Participants must have sufficient tumor tissue (fresh or archived) available for analysis of EphA2 tumor expression and other biomarkers.
* Adequate organ function (hematologic, renal, and hepatic).
* Negative pregnancy test for participants of childbearing potential (POCBP)
* Must be willing and able to comply with the protocol and study procedures and agree to participate in the study by providing written informed consent.

Exclusion Criteria

* Chemotherapy or radiotherapy within 14 days prior to the first dose of study treatment
* Experimental treatments within 28 days or 5 half-lives, whichever is longer, of first dose of nuzefatide study treatment
* Prior treatment with taxane therapy (e.g., paclitaxel) for pancreatic cancer or prior treatment with any MMAE-containing agent
* Known microsatellite instability-high (MSI-H) status and are eligible for immune checkpoint inhibitor therapy
* Prior toxicities must have resolved to Grade 1 per National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) v6.0
* Untreated central nervous system (CNS) metastases

Note: Additional protocol defined Inclusion/Exclusion criteria apply