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NCT06182072 · ClinicalTrials.gov registry record · Phase 1

ProAgio in Pancreatic Ductal Adenocarcinoma (PDAC)

A Phase 1 study of Pancreatic Ductal Adenocarcinoma (PDAC), sponsored by ProDa BioTech.

Recruiting
Registry status
Phase 1
Development phase
46
Enrollment target
1
Study location

NCT06182072 is a Phase 1 study of Pancreatic Ductal Adenocarcinoma (PDAC) that is actively recruiting participants, run by ProDa BioTech. The registered enrollment target is 46 participants, below the 294-participant average among 16 other Pancreatic Ductal Adenocarcinoma (PDAC) trials with a reported enrollment target (84% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06182072, a Phase 1 study of Pancreatic Ductal Adenocarcinoma (PDAC), is actively recruiting participants, sponsored by ProDa BioTech.

RECRUITING
Registry status
Phase 1
Development phase
46 participants
Enrollment target
1
Study location

Study Summary

This is an open-label Phase I/Ib dose-escalation, dose-expansion clinical trial of the safety, pharmacokinetics and clinical activity of ProAgio combined with gemcitabine, nab-paclitaxel (G-nP) or gemcitabine, nab-paclitaxel (G-nP) and atezolizumab in previously untreated subjects with metastatic pancreatic ductal adenocarcinoma (PDAC)

Interventions

  • DRUG ProAgio Dose Levels (DL) 1,2,3,4
  • DRUG Gemcitabine, nab paclitaxel

Study Locations (1)

Alabama

  • O'Neal Comprehensive Cancer Center, University of Alabama - Birmingham

Trial Details

FieldValue
Enrollment Target 46 participants
Start Date 2023-09-14
Est. Completion 2028-06-30
Phase Phase 1

Sponsor

ProDa BioTech

3 total trials

What the Registry Record Tells You About NCT06182072

The ClinicalTrials.gov registry entry for NCT06182072 describes a study currently listed as recruiting, categorized as Phase 1. The registered enrollment target is 46 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 294-participant average among 16 other Pancreatic Ductal Adenocarcinoma (PDAC) trials with a reported enrollment target (84% lower). The listed sponsor is ProDa BioTech, which has 3 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Pancreatic Ductal Adenocarcinoma (PDAC) appearing as the primary indexed condition, and to 2 interventions - of which ProAgio Dose Levels (DL) 1,2,3,4 is the first listed.

NCT06182072 reports 1 study location spanning 1 distinct geographic area - top geographies include Alabama.

Frequently Asked Questions

What is clinical trial NCT06182072 about?

NCT06182072 is a clinical study titled "ProAgio in Pancreatic Ductal Adenocarcinoma (PDAC)". This is an open-label Phase I/Ib dose-escalation, dose-expansion clinical trial of the safety, pharmacokinetics and clinical activity of ProAgio combined with gemcitabine, nab-paclitaxel (G-nP) or gemcitabine, nab-paclitaxel (G-nP) and atezolizumab in previously untreated subjects with metastatic pa...

What is the current status of trial NCT06182072?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 46 participants. The study started on 2023-09-14. Estimated completion is 2028-06-30.

What conditions does trial NCT06182072 study?

This clinical trial studies the following conditions: Pancreatic Ductal Adenocarcinoma (PDAC).

What interventions are being tested in trial NCT06182072?

The interventions under investigation include: ProAgio Dose Levels (DL) 1,2,3,4 (DRUG), Gemcitabine, nab paclitaxel (DRUG).

Who is sponsoring clinical trial NCT06182072?

This trial is sponsored by ProDa BioTech, which has 3 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06182072 being conducted?

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

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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