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

NCT03037645 · ClinicalTrials.gov registry record · Phase 1

Safety, PK, PD, and Antitumor Activity of Vecabrutinib (SNS-062) in B Lymphoid Cancers

A Phase 1 study, sponsored by Sunesis Pharmaceuticals.

Terminated
Registry status
Phase 1
Development phase
39
Enrollment target

NCT03037645: Clinical Trial Phase 1 study, sponsored by Sunesis Pharmaceuticals.

NCT03037645 is a Phase 1 study that was terminated before completion, run by Sunesis Pharmaceuticals. The registered enrollment target is 39 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (35% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT03037645, a Phase 1 study, was terminated before completion, sponsored by Sunesis Pharmaceuticals.

TERMINATED
Registry status
Phase 1
Development phase
39 participants
Enrollment target

Study Summary

This is an open-label Phase 1b/2 study in patients with chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL)or non hodgkin's lymphoma (NHL) who have failed prior standard of care therapies including a BTK inhibitor where one is approved for the indication.

Primary Outcome

To determine the Maximum Tolerated Dose (MTD) and/or Recommended Dose (RD)within the tested SNS-062 dose range. The MTD is the highest tested dose level at which ≥6 subjects have been treated and which is associated with a Cycle 1 dose limiting toxicity (DLT) in \<33% of the subjects. The RD may be the MTD or may be a lower dose.

Interventions

  • DRUG SNS-062

Trial Details

FieldValue
Enrollment Target 39 participants
Start Date 2017-04-28
Est. Completion 2020-08-31
Phase Phase 1
Sunesis Pharmaceuticals

13 total trials

Why NCT03037645 stopped before completion

NCT03037645 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 39 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (35% lower).

The record links to 0 conditions, and to 1 intervention - of which SNS-062 is the first listed.

NCT03037645 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03037645 about?

NCT03037645 is a clinical study titled "Safety, PK, PD, and Antitumor Activity of Vecabrutinib (SNS-062) in B Lymphoid Cancers". This is an open-label Phase 1b/2 study in patients with chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL)or non hodgkin's lymphoma (NHL) who have failed prior standard of care therapies including a BTK inhibitor where one is approved for the indication.

What is the current status of trial NCT03037645?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 39 participants. The study started on 2017-04-28. Estimated completion is 2020-08-31.

What interventions are being tested in trial NCT03037645?

The interventions under investigation include: SNS-062 (DRUG).

Who is sponsoring clinical trial NCT03037645?

This trial is sponsored by Sunesis Pharmaceuticals, which has 13 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03037645's enrollment target sits among peer trials

39 1191st of 2000 higher than 804 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

  • NCT03465592 · 39 participants · Phase 1

    Trial of Nivolumab Following Partially Human Leukocyte Antigen (HLA) Mismatched BMT in Children & Adults With Sarcoma

  • NCT03961776 · 39 participants

    Monitoring Treatment Response With On-board DWI During Neo-adjuvant Chemo-radiation for Rectal Cancer Using Magnetic Resonance-guided-radiotherapy Systems

  • NCT04050280 · 39 participants · Phase 2

    CLAG-GO for Patients With Persistent, Relapsed or Refractory AML

  • NCT04190862 · 39 participants · Phase 1

    E-CEL UVEC as an Adjunct Cell Therapy for Treatment of Anal Fistulas

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 NCT03037645, the US trial registry maintained by the National Library of Medicine. NCT03037645 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.