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Enrolling by invitationNCT07713901Updated Aug 4, 2026

Database Linkage Study to Evaluate the Risk of Medullary Thyroid Carcinoma

An observational study in Medullary Thyroid Carcinoma, sponsored by Novo Nordisk A/S. Enrolling by invitation at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-08-04.

Sponsored by Novo Nordisk A/S · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
93,600,000
Ages
18 Years and older
Sex
All
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Study summary

This is a database linkage study utilizing real-world data (RWD) to determine whether certain medicines used to treat type 2 diabetes (T2D) and support weight management (called GLP-1 RAs (Glucagon-like peptide-1 receptor agonists )) are linked to an increased risk of a rare cancer called medullary thyroid carcinoma (MTC). The purpose of this study is to compare how often medullary thyroid cancer occurs in people taking these medicines versus those taking other similar treatments. This study will use dispensed prescription claims and State Cancer Registry data to assess the risk of MTC.

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Conditions studied

  • Medullary Thyroid Carcinoma

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03

In context

Carcinoma, Medullary

65 studies on the registry are indexed under Carcinoma, Medullary; 17 are open to participants now.

This study's planned enrollment of 93,600,000 is above the median of 139 across 14 observational studies indexed under Carcinoma, Medullary.

Browse Carcinoma, Medullary studies →

Lead sponsor

Novo Nordisk A/S is the lead sponsor of 1,370 studies on the registry; 102 are open to participants now.

Of its 198 completed or terminated interventional studies of FDA-regulated products, 94 (47%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

The study population consists of adults aged 18 years and older in the United States who are receiving routine treatment for type 2 diabetes or weight management and are identified utilizing real-world data (RWD).

Inclusion criteria

  • 18 years or older during the year of index (date of qualifying medication)
  • In addition to index medication, greater than or equal to (≥) 1 dispensed medication (any class) within 24 months prior to the index date1
  • ≥1 dispensed medication (any class) after the index date and within 12 months of index date (12-month post-index period)
  • No evidence of cohort qualifying medication during 12-month before the index date
  • Reside in the US, including the District of Columbia (DC) during the study period
  • No missing values for year of birth

Exclusion criteria

Exclusion Criteria:

  • Patients with a diagnosis of MTC in the linked SCR data before their index date will not be included in the study.
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Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
93,600,000 participants (estimated)
Patient registry
No

Groups and cohorts

  • Long-acting GLP-1 RA Exposed Cohort

    Participants will be eligible for inclusion in this cohort if they have at least one dispensed prescription for a LA GLP-1 RA therapy during the study patient selection period.

    Other: No treatment given

  • T2D Active Comparator 1 Cohort

    Participants will be included in this cohort if they fill at least one dispensed prescription for SGLT2 or DPP-4 inhibitors during the study patient selection period with no evidence of SGLT2 or DPP-4 inhibitors and without LA GLP-1 RA use during the prior 12-month lookback period.

    Other: No treatment given

  • T2D Active Comparator 2 Cohort

    Participants will be included in this cohort if they fill at least one dispensed prescription for any antidiabetic medications (including SGLT2 or DPP-4 inhibitors), other than LA GLP-1 RA therapies during the study patient selection period with no evidence of the cohort qualifying medication during the prior 12-month lookback period.

    Other: No treatment given

  • Overweight/Obesity Active Comparator Cohort

    Participants will be included in this cohort if they fill at least one dispensed prescription for anti-obesity medications, other than LA GLP-1 RA therapies during the study patient selection period with no evidence of the cohort qualifying medication during the prior 12-month lookback period.

    Other: No treatment given

Interventions

  • OtherNo treatment given

    No treatment given

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What researchers measure

Primary outcomes

  1. Time to first occurence of Medullary Thyroid Carcinoma (MTC)

    Measured in number of days.

    Time frame: From day 1 up to 15 years

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Study locations

1 site
  • IQVIA
    Parsippany, New Jersey 07054, United States
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 4, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07713901
Lead sponsor
Novo Nordisk A/S
Responsible party
Sponsor
First posted
Jul 20, 2026
Start date
Dec 31, 2025
Primary completion
Dec 31, 2026 (estimated)
Completion
Dec 31, 2026 (estimated)
Last update
Aug 4, 2026

Study contacts

Clinical Transparency (dept. 2834)
study director · Novo Nordisk A/S

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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No contact was published for this record. The registry link below has the sponsor’s details.

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