PHN-012 in Advanced Solid Tumors

PHN-012 in Advanced Solid Tumors

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Purpose of this Study

This study has two parts. In the first part, called Phase 1a, doctors will test different amounts of a medicine called PHN-012 to find the safest dose. In the second part, called Phase 1b, doctors will see how well PHN-012 works against cancer. The medicine will be given through an IV, which means it goes into a vein. You will get the medicine every 21 days until your cancer gets worse or you have to stop because of bad side effects.

Who Can Participate?

Eligibility

To join this study, you must be 18 years or older and have already had at least one treatment for advanced disease. You can join if there are no other proven treatments left, if you cannot handle the side effects of standard treatments, or if you choose not to have standard treatment after learning about all your options.

Age Range

18-110

Sex/Genders

Male (cisgender)
Female (cisgender)
Non-binary or gender fluid
Transgender male
Transgender female
Looking for Healthy Participants
No

What is Involved?

Description

The study wants to find out if a medicine called PHN-012 is safe and if people can handle it well. It also wants to see how well PHN-012 works to fight advanced solid tumors, which are a type of cancer.

Locations

Duke University Hospital

Visit Timing

Weekdays

Compensation

No

Spanish Materials Available

No

Study Details

Full Title

First-in-Human, Phase 1 Study of PHN-012, an Antibody Drug Conjugate, in Patients with Advanced Solid Tumors

Principal Investigator

John
Strickler

Protocol Number

PRO00119232

NCT ID

NCT07127874

Phase

I

Enrollment Status

Pending Open to Enrollment