Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT04604132 · ClinicalTrials.gov registry record · Phase 1

Derazantinib Alone or in Combination With Paclitaxel, Ramucirumab or Atezolizumab in Gastric Adenocarcinoma

A Phase 1 study, sponsored by Basilea Pharmaceutica.

Terminated
Registry status
Phase 1
Development phase
47
Enrollment target

NCT04604132: Clinical Trial Phase 1 study, sponsored by Basilea Pharmaceutica.

NCT04604132 is a Phase 1 study that was terminated before completion, run by Basilea Pharmaceutica. The registered enrollment target is 47 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (22% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT04604132, a Phase 1 study, was terminated before completion, sponsored by Basilea Pharmaceutica.

TERMINATED
Registry status
Phase 1
Development phase
47 participants
Enrollment target

Study Summary

The purpose of this study was to evaluate the efficacy of derazantinib monotherapy or derazantinib in combination with paclitaxel and ramucirumab in patients with gastric adenocarcinoma (GAC) i.e. with human epidermal growth factor receptor 2 (HER2)-negative adenocarcinoma of the stomach or gastro-esophageal junction harboring fibroblast growth factor receptor 2 (FGFR2) genetic aberrations (GA).

Primary Outcome

ORR was defined by the percentage of patients with confirmed complete response (CR, which means disappearance of all target lesions) or partial response (PR, which means \>=30% decrease in the sum of the longest diameter of target lesions) by blinded independent central review (BICR) using the internationally recognized criteria for the radiological assessment in tumor response of solid tumors (RECIST 1.1). Overall Response (OR) = CR + PR. The patients in Cohort 1.1 had FGFR2 fusions or amplifi

Interventions

  • DRUG Derazantinib
  • DRUG Derazantinib-paclitaxel-ramucirumab combination

Trial Details

FieldValue
Enrollment Target 47 participants
Start Date 2020-10-06
Est. Completion 2022-11-21
Phase Phase 1
Basilea Pharmaceutica

21 total trials

Why NCT04604132 stopped before completion

NCT04604132 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 47 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (22% lower).

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

NCT04604132 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04604132 about?

NCT04604132 is a clinical study titled "Derazantinib Alone or in Combination With Paclitaxel, Ramucirumab or Atezolizumab in Gastric Adenocarcinoma". The purpose of this study was to evaluate the efficacy of derazantinib monotherapy or derazantinib in combination with paclitaxel and ramucirumab in patients with gastric adenocarcinoma (GAC) i.e. with human epidermal growth factor receptor 2 (HER2)-negative adenocarcinoma of the stomach or gastro-e...

What is the current status of trial NCT04604132?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 47 participants. The study started on 2020-10-06. Estimated completion is 2022-11-21.

What interventions are being tested in trial NCT04604132?

The interventions under investigation include: Derazantinib (DRUG), Derazantinib-paclitaxel-ramucirumab combination (DRUG).

Who is sponsoring clinical trial NCT04604132?

This trial is sponsored by Basilea Pharmaceutica, which has 21 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04604132's enrollment target sits among peer trials

47 1053rd of 2000 higher than 943 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT03313011 · 47 participants

    The Neurobiology of Two Distinct Types of Progressive Apraxia of Speech

  • NCT03467516 · 47 participants · Phase 2

    Adoptive Transfer of Tumor Infiltrating Lymphocytes for Metastatic Uveal Melanoma

  • NCT03886662 · 47 participants · Phase 1

    A Study of LB-100 in Patients With Low or Intermediate-1 Risk Myelodysplastic Syndromes (MDS)

  • NCT04013802 · 47 participants · Phase 1

    TETRAVI Multivirus CTL for Treatment of EBV, CMV, Adenovirus, and BK Infections Post Allogeneic SCT.

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT04604132, the US trial registry maintained by the National Library of Medicine. NCT04604132 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.