Phase 1 Pancreatic Cancer Trial, Recruiting NCT07261631 Sponsor: Novartis Pharmaceuticals Condition: Pancreatic Cancer
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Phase 1 Pancreatic Cancer Trial, Recruiting

NCT07261631
Recruiting Phase 1

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • Adults aged 18 or older who have been diagnosed with one of the following cancers that cannot be surgically removed and has either spread locally or to other parts of the body: pancreatic cancer, non-small cell lung cancer, hormone receptor-positive/HER2-negative breast cancer (ductal or lobular type), triple negative breast cancer, colorectal cancer, or soft tissue sarcoma (excluding certain types called GIST and Kaposi sarcoma — this last cancer type is for a specific part of the trial only)
  • People with pancreatic, lung, breast, or colorectal cancer whose disease has continued to grow or who could not tolerate standard treatments such as chemotherapy, immunotherapy, targeted therapy, hormone therapy, or CDK inhibitors, depending on the cancer type (unless those treatments were not appropriate for them to begin with)
  • People with colorectal cancer that has a specific genetic feature called MSI-H or dMMR must also have had their disease progress after, or been unable to tolerate, immunotherapy (unless they were not eligible for it)
  • People with soft tissue sarcoma whose disease has progressed after at least one round of systemic (whole-body) treatment (confirm with trial site)
  • People whose tumours show uptake of a specific imaging agent called 68Ga-NNS309, which would be assessed through a scan

Who may not be able to join:

  • People with blood counts that fall below certain levels — specifically, too few infection-fighting white blood cells, low red blood cell levels (anaemia), or too few platelets
  • People with a heart rhythm measurement (called QTcF interval) at or above a certain threshold, which may indicate a heart conduction issue
  • People whose kidneys are not functioning well enough, based on a calculation called eGFR falling below a set level
  • People with urinary blockage or bladder control problems that cannot be managed
  • People who have brain metastases (cancer that has spread to the brain) that are causing symptoms or that require direct treatment to the brain
  • People who have previously received any radioligand therapy (a type of treatment that delivers radiation directly to cancer cells)
  • People who have had radiation therapy within the four weeks before the first dose of the trial treatment

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 13 July 2026
Phase 1: approximately ~10% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Phone: 1-888-669-6682

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

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Trial details

Status
Recruiting
Phase
Phase 1
Registry
ClinicalTrials.gov
Start date
24 November 2025
Est. completion
9 May 2029

Where this trial is recruiting

🇨🇦 Canada 🇩🇰 Denmark 🇫🇷 France 🇩🇪 Germany 🇮🇱 Israel 🇸🇬 Singapore

Primary endpoints

Incidence and severity of dose limiting toxicities of 177Lu-DFC413; Incidence and severity of adverse events and serious adverse events of 177Lu-DFC413; Dose modifications for 177Lu-DFC413; Dose intensity for 177Lu-DFC413

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 13 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov