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NCT02910882 · ClinicalTrials.gov registry record · Phase 2

PEGPH20 Plus Gemcitabine With Radiotherapy in Patients With Localized, Unresectable Pancreatic Cancer

A Phase 2 study, sponsored by Scripps Health.

Terminated
Registry status
Phase 2
Development phase
4
Enrollment target

NCT02910882: Clinical Trial Phase 2 study, sponsored by Scripps Health.

NCT02910882 is a Phase 2 study that was terminated before completion, run by Scripps Health. The registered enrollment target is 4 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02910882, a Phase 2 study, was terminated before completion, sponsored by Scripps Health.

TERMINATED
Registry status
Phase 2
Development phase
4 participants
Enrollment target

Study Summary

This is a single arm phase II trial assessing the potential activity of combination PEGPH20 plus Gemcitabine with radiotherapy in ten patients with localized, unresectable pancreatic adenocarcinoma.

Primary Outcome

Adverse events will be assessed weekly, from Day1 Treatment through up to 8 weeks after the end of treatment. Safety will be assessed during the study by evaluation of AEs, clinical safety laboratory tests (hematology, blood chemistry (including C-reactive protein \[CRP\]), coagulation, urinalysis, and PEGPH20 immunogenicity), vital signs, 12-lead ECGs, and physical examinations. The severity of AEs will be graded by Investigators using the National Cancer Institute (NCI) Common Terminology Cri

Interventions

  • DRUG Gemcitabine
  • RADIATION Radiation
  • DRUG PEGylated Recombinant Human Hyaluronidase (PEGPH20)

Trial Details

FieldValue
Enrollment Target 4 participants
Start Date 2017-01-03
Est. Completion 2018-08-31
Phase Phase 2
Scripps Health

30 total trials

Why NCT02910882 stopped before completion

NCT02910882 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 4 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (97% lower).

The record links to 0 conditions, and to 3 interventions - of which Gemcitabine is the first listed.

NCT02910882 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02910882 about?

NCT02910882 is a clinical study titled "PEGPH20 Plus Gemcitabine With Radiotherapy in Patients With Localized, Unresectable Pancreatic Cancer". This is a single arm phase II trial assessing the potential activity of combination PEGPH20 plus Gemcitabine with radiotherapy in ten patients with localized, unresectable pancreatic adenocarcinoma.

What is the current status of trial NCT02910882?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 4 participants. The study started on 2017-01-03. Estimated completion is 2018-08-31.

What interventions are being tested in trial NCT02910882?

The interventions under investigation include: Gemcitabine (DRUG), Radiation (RADIATION), PEGylated Recombinant Human Hyaluronidase (PEGPH20) (DRUG).

Who is sponsoring clinical trial NCT02910882?

This trial is sponsored by Scripps Health, which has 30 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02910882's enrollment target sits among peer trials

4 2001st of 2000 the lowest of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT02910882, the US trial registry maintained by the National Library of Medicine. NCT02910882 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.