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Combination of XL092 and Cemiplimab in Anaplastic Thyroid Cancer

The purpose of this study is to look at the effectiveness of giving cemiplimab and XL092 before and after surgery for Anaplastic Thyroid Cancer.

Age & Gender

  • 18 years ~ 99 years
  • Male, Female, Gender Inclusive

Visit Availability

  • Standard business hours (M-F, 8-5)

Location

United States (Nationwide)

What will be asked of you

You will meet with the study team to determine if you are eligible for this study. The study team will review your medical history, exam, imaging, and labs. If you do not have archived tissue, you will need to have a tissue biopsy. If you are eligible for the study, you will start your treatment with the two study drugs (XL092 and cemiplimab). You will have surgery to remove your cancer. You may have radiation therapy, if the study team thinks it would help. After this, you will continue to take XL092 and cemiplimab for up to 2 years. After you finish treatment, you will follow up with your clinical team for up to 5 years.

In-person visits:
15+
Total length of participation:
5 years and 8 months

Looking for Specific Volunteers

Able to participate:

  • Diagnosis of Anaplastic Thyroid Cancer
  • Have archived tissue or is willing to have a tissue biopsy before starting treatment
  • Have BRAF V600E mutation in tumor
  • Have resectable, unresectable disease, or oligometastatic disease
  • Have adequate lab values per protocol

Not eligible if:

  • Pregnant or breastfeeding
  • Ongoing or recent significant autoimmune disease that requires treatment
  • Uncontrolled incurrent illness, such as active infection, congestive heart failure, uncontrolled hypertension, interstitial lung disease
  • Have clinically significant heart disease
  • Known infection of hepatitis B or C, HIV, or AID-related illness

Contact the Team

Visit Location

Contact & Visit Location

Primary Contact

Primary Visit Location

NC Cancer Hospital (Basnight)
UNC Hospitals / UNC Medical Center
101 Manning Dr, Chapel Hill, NC 27514, USA

Additional Study Information

Principal Investigator

Sid Sheth
LCCC - Clinical Trials

Study Type

Clinical or Medical
Interventional

Study Topics

Cancer (Thyroid and Other Gland/Endocrine)

IRB Number

24-3051

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