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NCT06600906 · ClinicalTrials.gov registry record

Hyperpolarized 13C MRI to Predict Response in Pancreatic Cancer

A clinical trial of Pancreatic Ductal Adenocarcinoma and Metastatic Pancreatic Ductal Adenocarcinoma, sponsored by University of California, San Francisco.

Recruiting
Registry status
70
Enrollment target
1
Study location

NCT06600906: Recruiting study of Pancreatic Ductal Adenocarcinoma and Metastatic Pancreatic Ductal Adenocarcinoma, sponsored by University of California, San Francisco.

NCT06600906 is a study of Pancreatic Ductal Adenocarcinoma and Metastatic Pancreatic Ductal Adenocarcinoma that is actively recruiting participants, run by University of California, San Francisco. The registered enrollment target is 70 participants, below the 600-participant average among 84 other Pancreatic Ductal Adenocarcinoma trials with a reported enrollment target (88% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06600906, a study of Pancreatic Ductal Adenocarcinoma and Metastatic Pancreatic Ductal Adenocarcinoma, is actively recruiting participants, sponsored by University of California, San Francisco.

RECRUITING
Registry status
70 participants
Enrollment target
1
Study location

Study Summary

This study evaluates an investigational scan called hyperpolarized carbon-13 pyruvate magnetic resonance imaging (MRI) in assessing treatment response in patients with pancreatic ductal carcinoma (PDA) that has spread to nearby tissue or lymph nodes (locally advanced) or that has spread from where it first started (primary site) to other places in the body (metastatic). MRI is a standard scan that helps doctors see tumors, organs, tissue, and bone. Standard contrast agents (e.g., gadolinium) are sometimes used to help make the scan images brighter, or easier to see. Hyperpolarized carbon-13 pyruvate is an experimental contrast agent that is different from standard MRI contrast in that it provides information on how a tumor processes nutrients. Hyperpolarized carbon-13 pyruvate MRI scans may work better than MRI with standard contrast agents in predicting how PDA tumors respond to treatment.

Primary Outcome

The best objective response based on clinical imaging according to Response Evaluation Criteria in Solid Tumors (RECIST) version 1.11 will be reported

Interventions

  • DRUG Hyperpolarized 13C-Pyruvate
  • PROCEDURE Magnetic Resonance Imaging (MRI)
  • PROCEDURE Computed tomography (CT)

Study Locations (1)

California

  • University of California, San Francisco - San Francisco

Trial Details

FieldValue
Enrollment Target 70 participants
Start Date 2024-10-01
Est. Completion 2032-09-01

What NCT06600906 shows while recruiting

NCT06600906 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 70 participants, a relatively small participant target, below the 600-participant average among 84 other Pancreatic Ductal Adenocarcinoma trials with a reported enrollment target (88% lower).

The record links to 3 conditions, with Pancreatic Ductal Adenocarcinoma appearing as the primary indexed condition, and to 3 interventions - of which Hyperpolarized 13C-Pyruvate is the first listed.

NCT06600906 reports a single indexed study location in California.

Frequently Asked Questions

What is clinical trial NCT06600906 about?

NCT06600906 is a clinical study titled "Hyperpolarized 13C MRI to Predict Response in Pancreatic Cancer". This study evaluates an investigational scan called hyperpolarized carbon-13 pyruvate magnetic resonance imaging (MRI) in assessing treatment response in patients with pancreatic ductal carcinoma (PDA) that has spread to nearby tissue or lymph nodes (locally advanced) or that has spread from where i...

What is the current status of trial NCT06600906?

This trial is currently recruiting. The enrollment target is 70 participants. The study started on 2024-10-01. Estimated completion is 2032-09-01.

What conditions does trial NCT06600906 study?

This clinical trial studies the following conditions: Pancreatic Ductal Adenocarcinoma, Metastatic Pancreatic Ductal Adenocarcinoma, Locally Advanced Pancreatic Ductal Adenocarcinoma.

What interventions are being tested in trial NCT06600906?

The interventions under investigation include: Hyperpolarized 13C-Pyruvate (DRUG), Magnetic Resonance Imaging (MRI) (PROCEDURE), Computed tomography (CT) (PROCEDURE).

Who is sponsoring clinical trial NCT06600906?

This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06600906 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Pancreatic Ductal Adenocarcinoma

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06600906's enrollment target sits among peer trials

70 49th of 84 higher than 35 of 84 other Pancreatic Ductal Adenocarcinoma trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Pancreatic Ductal Adenocarcinoma trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06600906, the US trial registry maintained by the National Library of Medicine. NCT06600906 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.