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NCT02501902 · ClinicalTrials.gov registry record · Phase 1

Dose-Escalation Study Of Palbociclib + Nab-Paclitaxel In mPDAC

A Phase 1 study, sponsored by Pfizer.

Completed
Registry status
Phase 1
Development phase
76
Enrollment target

NCT02501902: Completed Phase 1 study, sponsored by Pfizer.

NCT02501902 is a Phase 1 study that has completed, run by Pfizer. The registered enrollment target is 76 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (27% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02501902, a Phase 1 study, has completed, sponsored by Pfizer.

COMPLETED
Registry status
Phase 1
Development phase
76 participants
Enrollment target

Study Summary

This is a Phase 1, open label, multi center, multiple dose, dose escalation, safety, pharmacokinetic and pharmacodynamic study of palbociclib in combination with nab-P, in sequential cohorts of adult patients with mPDAC, with MTD expansion cohort(s). Approximately 30-60 patients are expected to be enrolled in the overall study.

Primary Outcome

Adverse events (AEs) considered as dose limiting toxicities (DLTs) included: hematologic: Grade 4 neutropenia lasting \>4 days; Febrile neutropenia (defined as neutropenia Grade\>=3 \[absolute neutrophil count {ANC}\<1000 cells/cubic millimeter {mm\^3}\] and a body temperature \>=38.5 \[degrees centigrade\]℃) requiring antibiotic or antifungal treatment; any Grade 4 thrombocytopenia (\<25000/mm\^3 or 25.0\*10\^9/\[liter\]L). Non-hematologic: Grade \>=3 toxicities, except those that had not been

Interventions

  • DRUG Nab-Paclitaxel
  • DRUG Palbociclib

Trial Details

FieldValue
Enrollment Target 76 participants
Start Date 2015-11-23
Est. Completion 2018-12-27
Phase Phase 1
Pfizer

1,845 total trials

What the finished NCT02501902 record still lists

NCT02501902 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 76 participants, a relatively small participant target, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (27% higher).

The record links to 0 conditions, and to 2 interventions - of which Nab-Paclitaxel is the first listed.

NCT02501902 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02501902 about?

NCT02501902 is a clinical study titled "Dose-Escalation Study Of Palbociclib + Nab-Paclitaxel In mPDAC". This is a Phase 1, open label, multi center, multiple dose, dose escalation, safety, pharmacokinetic and pharmacodynamic study of palbociclib in combination with nab-P, in sequential cohorts of adult patients with mPDAC, with MTD expansion cohort(s). Approximately 30-60 patients are expected to be e...

What is the current status of trial NCT02501902?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 76 participants. The study started on 2015-11-23. Estimated completion is 2018-12-27.

What interventions are being tested in trial NCT02501902?

The interventions under investigation include: Nab-Paclitaxel (DRUG), Palbociclib (DRUG).

Who is sponsoring clinical trial NCT02501902?

This trial is sponsored by Pfizer, which has 1,845 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02501902's enrollment target sits among peer trials

76 705th of 2000 higher than 1,290 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 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 NCT02501902, the US trial registry maintained by the National Library of Medicine. NCT02501902 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.