deltatrials
Terminated PHASE2 INTERVENTIONAL 2-arm NCT03559387

Randomized Phase 2, Dose-finding Efficacy, Safety Study of ANF-RHO™ Versus Neulasta® in Chemotherapy-Induced Neutropenia

A Randomized and Open-label Dose-finding, Ph. 2, Efficacy, Safety, and Pharmacokinetic Study of Once-per-cycle Prophylactic Injections of ANF-RHO™ Versus Pegfilgrastim (Neulasta®) in Non-metastatic Breast Cancer Patients at High-risk of Chemotherapy-induced Neutropenia

Sponsor: Prolong Pharmaceuticals

Updated 5 times since 2018 Last updated: Feb 8, 2019 Started: Aug 3, 2017 Primary completion: Apr 18, 2018 Completion: May 22, 2018
This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

Terminated

Study redesign

A PHASE2 clinical study on Chemotherapy-induced Neutropenia, this trial is terminated or withdrawn. The trial is conducted by Prolong Pharmaceuticals and has accumulated 5 data snapshots since 2017. Longitudinal tracking of this trial contributes to a broader understanding of treatment development timelines.

Status Flow

~Jul 2018 – ~Mar 2019 · 8 months · monthly snapshotRecruiting~Mar 2019 – ~Jan 2021 · 22 months · monthly snapshotTerminated~Jan 2021 – ~Jul 2024 · 42 months · monthly snapshotTerminated~Jul 2024 – ~Sep 2024 · 2 months · monthly snapshotTerminated~Sep 2024 – present · 24 months · monthly snapshotTerminated

Change History

5 versions recorded
  1. Sep 2024 — Present [monthly]

    Terminated PHASE2

  2. Jul 2024 — Sep 2024 [monthly]

    Terminated PHASE2

  3. Jan 2021 — Jul 2024 [monthly]

    Terminated PHASE2

  4. Mar 2019 — Jan 2021 [monthly]

    Terminated PHASE2

    Status: RecruitingTerminated

  5. Jul 2018 — Mar 2019 [monthly]

    Recruiting PHASE2

    First recorded

Aug 2017

Trial started

Per CT.gov start date — pre-dates our first snapshot

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:
  • Prolong Pharmaceuticals
Data source: Prolong Pharmaceuticals

For direct contact, visit the study record on ClinicalTrials.gov .