Study of XB010 in Subjects With Solid Tumors

Description

This is a FIH study is to evaluate the safety, tolerability, PK, immunogenicity, and preliminary antitumor activity of XB010 as a single agent and in combination with pembrolizumab in subjects with locally advanced or metastatic solid tumors for whom alternative therapies do not exist or available therapies are intolerable or no longer effective.

Conditions

Locally Advanced or Metastatic Solid Tumors

Study Overview

Study Details

Study overview

This is a FIH study is to evaluate the safety, tolerability, PK, immunogenicity, and preliminary antitumor activity of XB010 as a single agent and in combination with pembrolizumab in subjects with locally advanced or metastatic solid tumors for whom alternative therapies do not exist or available therapies are intolerable or no longer effective.

A Dose-Escalation and Expansion Study of XB010 as a Single Agent and Combination Therapy in Subjects With Locally Advanced or Metastatic Solid Tumors

Study of XB010 in Subjects With Solid Tumors

Condition
Locally Advanced or Metastatic Solid Tumors
Intervention / Treatment

-

Contacts and Locations

Duarte

Exelixis Clinical Site #4, Duarte, California, United States, 91010

Huntersville

Exelixis Clinical Site #3, Huntersville, North Carolina, United States, 28078

Austin

Exelixis Clinical Site #1, Austin, Texas, United States, 78758

Fairfax

Exelixis Clinical Site #2, Fairfax, Virginia, United States, 22031

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

    Ages Eligible for Study

    18 Years to

    Sexes Eligible for Study

    ALL

    Accepts Healthy Volunteers

    No

    Collaborators and Investigators

    Exelixis,

    Study Record Dates

    2027-10-20