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NCT02014441 · ClinicalTrials.gov registry record · Phase 2

Single-arm Trial to Evaluate the Biodistribution and Shedding of Talimogene Laherparepvec

A Phase 2 study, sponsored by Amgen.

Completed
Registry status
Phase 2
Development phase
61
Enrollment target

NCT02014441: Completed Phase 2 study, sponsored by Amgen.

NCT02014441 is a Phase 2 study that has completed, run by Amgen. The registered enrollment target is 61 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (54% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02014441, a Phase 2 study, has completed, sponsored by Amgen.

COMPLETED
Registry status
Phase 2
Development phase
61 participants
Enrollment target

Study Summary

The primary objective was to estimate the proportion of participants with detectable talimogene laherparepvec deoxyribonucleic acid (DNA) in the blood and urine at any time after administration of talimogene laherparepvec within the first 3 cycles.

Primary Outcome

Talimogene laherparepvec DNA was measured using a quantitative polymerase chain reaction (qPCR) method. The percentage of participants with detectable talimogene laherparepvec DNA in blood or urine at any time during cycles 1 to 3 is reported. The first cycle was 21 days in length, and subsequent cycles were 14 days in length.

Interventions

  • DRUG Talimogene laherparepvec

Trial Details

FieldValue
Enrollment Target 61 participants
Start Date 2014-04-07
Est. Completion 2018-04-19
Phase Phase 2
Amgen

558 total trials

What the finished NCT02014441 record still lists

NCT02014441 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 61 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (54% lower).

The record links to 0 conditions, and to 1 intervention - of which Talimogene laherparepvec is the first listed.

NCT02014441 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02014441 about?

NCT02014441 is a clinical study titled "Single-arm Trial to Evaluate the Biodistribution and Shedding of Talimogene Laherparepvec". The primary objective was to estimate the proportion of participants with detectable talimogene laherparepvec deoxyribonucleic acid (DNA) in the blood and urine at any time after administration of talimogene laherparepvec within the first 3 cycles.

What is the current status of trial NCT02014441?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 61 participants. The study started on 2014-04-07. Estimated completion is 2018-04-19.

What interventions are being tested in trial NCT02014441?

The interventions under investigation include: Talimogene laherparepvec (DRUG).

Who is sponsoring clinical trial NCT02014441?

This trial is sponsored by Amgen, which has 558 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02014441's enrollment target sits among peer trials

61 1026th of 2000 higher than 974 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 NCT02014441, the US trial registry maintained by the National Library of Medicine. NCT02014441 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.