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NCT03105336 · ClinicalTrials.gov registry record · Phase 2

A Study of Axicabtagene Ciloleucel in Participants With Relapsed/Refractory Indolent Non-Hodgkin Lymphoma

A Phase 2 study, sponsored by Kite, A Gilead Company.

Completed
Registry status
Phase 2
Development phase
159
Enrollment target

NCT03105336: Completed Phase 2 study, sponsored by Kite, A Gilead Company.

NCT03105336 is a Phase 2 study that has completed, run by Kite, A Gilead Company. The registered enrollment target is 159 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (20% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03105336, a Phase 2 study, has completed, sponsored by Kite, A Gilead Company.

COMPLETED
Registry status
Phase 2
Development phase
159 participants
Enrollment target

Study Summary

The goal of this study is to assess whether axicabtagene ciloleucel improves the clinical outcome in participants with relapsed or refractory indolent non-Hodgkin lymphoma (r/r) iNHL.

Primary Outcome

OR:CR (complete metabolic response (CMR)+complete radiological response (CRR))+PR (partial MR response (PMR) +partial RR(PRR)).CMR: score 1(no uptake above background)/2(uptake≤mediastinum)/3(uptake \>mediastinum but ≤liver)with/without a residual mass on positron emission tomography 5-point scale;no new lesions,CRR:target nodes/nodal masses regressed to ≤1.5 cm in longest transverse diameter of lesion (LDi);no extralymphatic sites of disease;absent non-measured lesion(NMLs);organ enlargement re

Interventions

  • DRUG Cyclophosphamide
  • DRUG Fludarabine
  • BIOLOGICAL Axicabtagene ciloleucel

Trial Details

FieldValue
Enrollment Target 159 participants
Start Date 2017-06-06
Est. Completion 2024-12-20
Phase Phase 2
Kite, A Gilead Company

28 total trials

What the finished NCT03105336 record still lists

NCT03105336 is an interventional study that assigns participants to a tested intervention. The registered 159 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (20% higher).

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

NCT03105336 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03105336 about?

NCT03105336 is a clinical study titled "A Study of Axicabtagene Ciloleucel in Participants With Relapsed/Refractory Indolent Non-Hodgkin Lymphoma". The goal of this study is to assess whether axicabtagene ciloleucel improves the clinical outcome in participants with relapsed or refractory indolent non-Hodgkin lymphoma (r/r) iNHL.

What is the current status of trial NCT03105336?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 159 participants. The study started on 2017-06-06. Estimated completion is 2024-12-20.

What interventions are being tested in trial NCT03105336?

The interventions under investigation include: Cyclophosphamide (DRUG), Fludarabine (DRUG), Axicabtagene ciloleucel (BIOLOGICAL).

Who is sponsoring clinical trial NCT03105336?

This trial is sponsored by Kite, A Gilead Company, which has 28 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03105336's enrollment target sits among peer trials

159 442nd of 2000 higher than 1,558 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 NCT03105336, the US trial registry maintained by the National Library of Medicine. NCT03105336 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.