Phase 1 Pancreatic Cancer Trial, Recruiting NCT06562192 Sponsor: Novartis Pharmaceuticals Condition: Pancreatic Cancer
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Phase 1 Pancreatic Cancer Trial, Recruiting

NCT06562192
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:

  • People aged 18 or older
  • People with pancreatic cancer (PDAC) that has spread or cannot be surgically removed, and whose cancer has continued to grow after chemotherapy, or who were unable to tolerate or were not eligible for chemotherapy
  • People with non-small cell lung cancer (NSCLC) that has spread or cannot be surgically removed, whose cancer has continued to grow after appropriate treatments (chemotherapy, immunotherapy, or targeted therapy depending on their cancer type), or who were unable to tolerate or were not eligible for those treatments
  • People with a type of breast cancer called HR+/HER2- (ductal or lobular) that has spread or cannot be surgically removed, and whose cancer has continued to grow after at least 2 previous treatments, or who were unable to tolerate or were not eligible for those treatments
  • People with triple-negative breast cancer (TNBC) that has spread or cannot be surgically removed, and whose cancer has continued to grow after at least 2 previous treatments, or who were unable to tolerate or were not eligible for those treatments
  • People with colorectal cancer (CRC) that has spread or cannot be surgically removed — this applies to the early dose-testing part of the trial only — whose cancer has continued to grow after chemotherapy and, in certain cases, after immunotherapy as well (confirm with trial site)
  • People whose tumours show uptake of a specific imaging agent called 68Ga-NNS309 on a scan

Who may not be able to join:

  • People with low blood cell counts, including low white blood cells, low red blood cells (haemoglobin below 9 g/dL), or low platelets
  • People with a specific type of irregular heart rhythm reading (a prolonged QTcF interval of 470 milliseconds or more on an ECG)
  • People whose kidneys are not filtering well enough (creatinine clearance below 60 mL/min)
  • People with urinary tract blockages or urinary incontinence that cannot be managed
  • People who have received radiation therapy within 4 weeks before the first dose of the trial treatment
  • Other criteria set out in the study protocol may also apply (confirm with trial site)

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 28 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

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 1
Registry
ClinicalTrials.gov
Start date
15 October 2024
Est. completion
15 January 2031

Where this trial is recruiting

🇧🇪 Belgium 🇨🇦 Canada 🇫🇷 France 🇩🇪 Germany 🇮🇱 Israel 🇮🇹 Italy 🇳🇱 Netherlands 🇪🇸 Spain 🇨🇭 Switzerland 🇺🇸 United States

Primary endpoints

Number of patients with dose limiting toxicities of [177Lu]Lu-NNS309; Incidence and severity of adverse events and serious adverse events of [177Lu]Lu-NNS309; Dose modifications for [177Lu]Lu-NNS309; Dose intensity for [177Lu]Lu-NNS309

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: 28 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