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NCT07109414 · ClinicalTrials.gov registry record · Phase 2

Trial of NP-G2-044 (Prilukae) Combined With PLD for Treatment of Platinum-Resistant Ovarian Cancer (ULTIMUS-1)

A Phase 2 study of Platinum-resistant Ovarian Cancer, sponsored by Novita Pharmaceuticals.

Active
Registry status
Phase 2
Development phase
380
Enrollment target
6
Study locations

NCT07109414 is a Phase 2 study of Platinum-resistant Ovarian Cancer that is active but no longer recruiting, run by Novita Pharmaceuticals. The registered enrollment target is 380 participants, above the 164-participant average among 17 other Platinum-resistant Ovarian Cancer trials with a reported enrollment target (132% higher). The trial reports 6 study locations across 6 states.

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The verdict

NCT07109414, a Phase 2 study of Platinum-resistant Ovarian Cancer, is active but no longer recruiting, sponsored by Novita Pharmaceuticals.

ACTIVE NOT RECRUITING
Registry status
Phase 2
Development phase
380 participants
Enrollment target
6
Study locations

Study Summary

The purpose of the study is to identify the optimal dose level of NP-G2-044 in combination with standard of care (SOC) pegylated liposomal doxorubicin (PLD), and to compare the efficacy and safety of NP-G2-044+PLD vs. PLD alone in participants with platinum-resistant ovarian cancer (PROC).

Interventions

  • DRUG PLD
  • DRUG NP-G2-044

Study Locations (6)

Arizona

  • HonorHealth Cancer Care - Phoenix

Louisiana

  • Trials365 - Shreveport

New Mexico

  • Optimum Clinical Research Group, LLC - Albuquerque

Pennsylvania

  • University of Pennsylvania Health System, Perelman Center for Advanced Medicine - Philadelphia

Utah

  • Utah Cancer Specialists - Salt Lake City

Wisconsin

  • University Of Wisconsin Carbone Cancer Center - Madison

Trial Details

FieldValue
Enrollment Target 380 participants
Start Date 2025-12-29
Est. Completion 2029-10-24
Phase Phase 2

Sponsor

Novita Pharmaceuticals

3 total trials

What the Registry Record Tells You About NCT07109414

The ClinicalTrials.gov registry entry for NCT07109414 describes a study currently listed as active not recruiting, categorized as Phase 2. The registered enrollment target is 380 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 164-participant average among 17 other Platinum-resistant Ovarian Cancer trials with a reported enrollment target (132% higher). The listed sponsor is Novita Pharmaceuticals, which has 3 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Platinum-resistant Ovarian Cancer appearing as the primary indexed condition, and to 2 interventions - of which PLD is the first listed.

NCT07109414 reports 6 study locations spanning 6 distinct geographic areas - top geographies include Arizona, Louisiana, New Mexico.

Frequently Asked Questions

What is clinical trial NCT07109414 about?

NCT07109414 is a clinical study titled "Trial of NP-G2-044 (Prilukae) Combined With PLD for Treatment of Platinum-Resistant Ovarian Cancer (ULTIMUS-1)". The purpose of the study is to identify the optimal dose level of NP-G2-044 in combination with standard of care (SOC) pegylated liposomal doxorubicin (PLD), and to compare the efficacy and safety of NP-G2-044+PLD vs. PLD alone in participants with platinum-resistant ovarian cancer (PROC).

What is the current status of trial NCT07109414?

This trial is currently active not recruiting. It is a Phase 2 study. The enrollment target is 380 participants. The study started on 2025-12-29. Estimated completion is 2029-10-24.

What conditions does trial NCT07109414 study?

This clinical trial studies the following conditions: Platinum-resistant Ovarian Cancer.

What interventions are being tested in trial NCT07109414?

The interventions under investigation include: PLD (DRUG), NP-G2-044 (DRUG).

Who is sponsoring clinical trial NCT07109414?

This trial is sponsored by Novita Pharmaceuticals, which has 3 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07109414 being conducted?

This trial has 6 study locations across Arizona, Louisiana, New Mexico, Pennsylvania, Utah. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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