Skip to content

An Active Surveillance Program for Cases of Medullary Thyroid Carcinoma (MTC)

Medullary Thyroid Carcinoma Surveillance Study: A Case-Series Registry

Status
Enrolling by invitation
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01511393
Enrollment
6750
Registered
2012-01-18
Start date
2012-01-31
Completion date
2039-12-31
Last updated
2023-06-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetes, Diabetes Mellitus, Type 2, Medullary Thyroid Carcinoma, Weight Management

Keywords

GLP1, Glucagon like peptide, liraglutide, exenatide extended release, dulaglutide, semaglutide, semaglutide tablets

Brief summary

This study is conducted in the United States of America (USA). The aim of the study is to monitor the number of annual new adult cases of medullary thyroid carcinoma (MTC) and to establish a registry for these new cases in order to identify any possible increase related to the introduction of liraglutide, exenatide once-weekly, and other GLP-1 receptor agonists into the US market.

Detailed description

This active surveillance program will monitor for any signal indicating a possible association between treatment with long-acting GLP-1 RAs and the development of MTC in the United States population. Given the very low incidence of MTC in the general population, the expected rate of exposure to long-acting GLP-1 RAs, the anticipated long latency of the potential outcome under study and the limited data on underlying risk factors for development of MTC other than RET proto-oncogene mutations, an active surveillance program is the most efficient means of identifying a possible association between MTC and products in the long-acting GLP-1 RAs class. Given the uncertainty of the association of MTC in humans treated with these drugs, a study duration of at least fifteen years from the time of market introduction of the first long-acting GLP-1 RA was thought to provide evidence of an association, if one exists. If such an association is identified, a case-control study will be initiated to quantify the association. The MTC registry is a Food and Drug Administration (FDA) post-marketing requirement for long-acting GLP-1 RA products. Because of the rarity of MTC and in order to minimize inconvenience to patients, physicians, and state cancer registries, FDA encouraged sponsors of long-acting GLP-1 RAs to work collaboratively to conduct this registry. Consequently, the MTC Registry Consortium has been formed for this purpose. The MTC Registry Consortium refers to the Sponsors with approved long-acting GLP-1 RAs who have a contractual agreement to participate in the MTC Registry. This active surveillance program for cases of MTC will be conducted with assistance from the North American Association of Central Cancer Registries (NAACCR). NAACCR is a collaborative umbrella organization for cancer registries, government agencies, professional organizations, and private groups in North America interested in improving the quality and use of cancer registry data. All of the central cancer registries in the U.S. and Canada are members of NAACCR, including those that participate in SEER.

Interventions

OTHERNo treatment given

None. Non-interventional study.

Sponsors

AstraZeneca
CollaboratorINDUSTRY
Eli Lilly and Company
CollaboratorINDUSTRY
United BioSource, LLC
CollaboratorINDUSTRY
Novo Nordisk A/S
Lead SponsorINDUSTRY

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* A record of medullary thyroid carcinoma (MTC) identified from state/regional population-based cancer registries * At least 18 years or older. There are no other inclusion or

Exclusion criteria

.

Design outcomes

Primary

MeasureTime frame
Annual incidence of MTC in the US to identify any possible increase related to the introduction of liraglutide, exenatide once-weekly, and other GLP-1 receptor agonists into the US market.Up to 15 years

Secondary

MeasureTime frame
Family history of cancer (including history of MEN2A or MEN 2B, history of FMTC, history of RET proto-oncogene mutations), Patient demographic characteristics, Patient prior history of thyroid diseasesUp to 15 years
Dose and Duration of use of all previous diabetes medication exposures (including long acting and short acting GLP-1 receptor agonists, DPP4 inhibitors, and insulin)Up to 15 years
Dose and Duration of use of all previous weight management drugs (including long acting GLP-1 receptor agonists).Up to 15 years
Lifestyle factors such as smoking and alcohol useUp to 15 years
Environmental exposures (occupational history, radioiodine exposure, nuclear fallout)Up to 15 years

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 17, 2026