RECRUITING

A Study Evaluating the Safety and Efficacy of HB0036 in Subjects With Advanced Solid Tumors

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

It is a Phase I/II, Open-label, Multicenter Study to Evaluate the Safety, Pharmacokinetics, Pharmacodynamics, and Efficacy of HB0036 in Subjects with Advanced Solid Tumors

Official Title

A Phase I/II, Open-label, Multicenter Study to Evaluate the Safety, Pharmacokinetics, Pharmacodynamics, and Efficacy of HB0036 in Subjects With Advanced Solid Tumors

Quick Facts

Study Start:2022-08-25
Study Completion:2024-08-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05417321

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.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. Age 18 years or older
  2. Willing and able to provide informed consent
  3. Able to understand and follow study procedures
  4. Stable medical condition
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Contact

Jingjing Wang, Master
CONTACT
021-51320053
jingjing.wang@huaota.com
Yang Zheng, MD
CONTACT
021-51320053
yang.zheng@huaota.com

Principal Investigator

Yang Yang, MD/PHD
STUDY_DIRECTOR
Shanghai Huaota Biopharmaceutical Co., Ltd.

Study Locations (Sites)

Horizon Oncology
Lafayette, Indiana, 47905
United States
Next Oncology
San Antonio, Texas, 78229
United States
Summit Cancer Centers
Spokane, Washington, 99216
United States

Collaborators and Investigators

Sponsor: Shanghai Huaota Biopharmaceutical Co., Ltd.

  • Yang Yang, MD/PHD, STUDY_DIRECTOR, Shanghai Huaota Biopharmaceutical Co., Ltd.

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2022-08-25
Study Completion Date2024-08-01

Study Record Updates

Study Start Date2022-08-25
Study Completion Date2024-08-01

Terms related to this study

Additional Relevant MeSH Terms

  • Advanced Solid Tumor
  • NSCLC