PumaRx Registry Trial

Part of paid clinical trials in Coral Gables, Florida.

Sponsor
RenovoRx
Study ID
NCT06805461
Status
Recruiting

Conditions

  • Solid Tumors

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • RenovoCath® — DEVICE
    Intra-arterial catheter delivery of chemotherapy agents for the collection of real-world data.

Study Details

This study is a multicenter, observational, post-marketing, registry study designed to track the safety and performance of the RenovoCath® device and assess survival outcomes in patients diagnosed with solid tumors who are treated with localized intra-arterial (IA) delivery of therapeutic agents to solid tumors using the RenovoCath® catheter.

Key Dates

Start date
Aug 1, 2025
Status verified
Oct 2025
Primary completion
Sep 3, 2029
Completion
Sep 3, 2029

Study Design

Enrollment
1,000 participants (estimated)

Arms

  • Arm: Patients receiving Intra-Arterial treatment with RenovoCath
    Patients receiving Intra-Arterial treatment with RenovoCath

Primary Outcome Measure

Safety of RenovoCath® as assessed by the number of participants experiencing adverse events related to the chemotherapy agents administered using RenovoCath. [ Time Frame: From the time of the first treatment, until 30 days after the last treatment ]

Central Contacts

Locations (3)

FacilityCityStateZIPSite coordinators
Baptist Health South FloridaCoral GablesFlorida33143
Dr. Gandhi
University of Pennsylvania Medical CenterPittsburghPennsylvania15213
Dr. Novelli
The University of Vermont Medical CenterBurlingtonVermont05401
Dr. O'Neill

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