Source: ClinicalTrials.gov — U.S. National Library of Medicine — A database of privately and publicly funded clinical studies conducted around the world (U.S. National Library of Medicine, public domain).
This page lists clinical trials related to Thyroid Diseases from the ClinicalTrials.gov database.
Trial Summary
- Total studies: 50
- Recruiting: 27
- Active, not recruiting: 10
- Completed: 10
- Other: 3
Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.
Recruiting Trials
NCT01005654 — Prospective Comprehensive Molecular Analysis of Endocrine Neoplasms
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 2415 |
| Study Type | OBSERVATIONAL |
| Conditions | Endocrine Tumors; Thyroid Neoplasms; Parathyroid Neoplasms; Adrenal Neoplasm; Neuroblastoma |
Background:
- Endocrine neoplasms (tumors) are among the fastest growing tumors in incidence in the United States. Furthermore, it is often difficult to distinguish between benign or malignant tumors in cancers of the thyroid, parathyroid, adrenal gland, and pancreas. More research is needed to improve detection and treatment options for patients who develop these kinds of cancer.
- Researcher…
NCT01109420 — Clinical and Genetic Studies in Familial Non-medullary Thyroid Cancer
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) |
| Enrollment | 500 |
| Study Type | OBSERVATIONAL |
| Conditions | Non-Medullary Thyroid Cancer |
Background:
- Researchers are studying types of thyroid cancer that seem to cluster in families. Non-medullary thyroid cancer accounts for the vast majority of all types of thyroid cancer, but little is known about possible genes that may cause the cancer. More research is needed to develop the best ways to screen for familial non-medullary thyroid cancer (FNMTC) so that it can be diagnosed a…
NCT01247597 — DICER1-related Pleuropulmonary Blastoma Cancer Predisposition Syndrome: A Natural History Study
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 1500 |
| Study Type | OBSERVATIONAL |
| Conditions | Pleuropulmonary Blastoma; Cystic Nephroma; Ovarian Sertoli-Leydig Cell Tumors; Ocular Medulloepithelioma; Nasal Chondromesenchymal Hamartoma |
Background:
- Pleuropulmonary blastoma (PPB) is a rare fast-growing lung tumor that is associated with other, rare tumor types. Most cases of PPB appear in children younger than 6 years of age. Recently, it has been shown that this condition can be inherited (e.g., mutation of the DICER1 gene). Researchers are studying both clinical and genetic aspects of this newly described condition. They …
NCT01660984 — Natural History Study of Children and Adults With Medullary Thyroid Cancer
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 259 |
| Study Type | OBSERVATIONAL |
| Conditions | Medullary Thyroid Cancer |
Background:
- Medullary thyroid cancer (MTC) is a rare cancer of the thyroid gland. In children and adults, it is often part of a condition called Multiple Endocrine Neoplasia 2 (MEN2). MEN2 is usually caused by a genetic mutation, and it can cause a number of problems in addition to MTC. These problems include adrenal gland tumors, hormone changes, and problems with the bones and other organ…
NCT02012699 — Integrated Cancer Repository for Cancer Research
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Nebraska |
| Enrollment | 999999 |
| Study Type | OBSERVATIONAL |
| Conditions | Pancreatic Cancer; Thyroid Cancer; Lung Cancer; Esophageal Cancer; Thymus Cancer |
The iCaRe2 is a multi-institutional resource created and maintained by the Fred & Pamela Buffett Cancer Center to collect and manage standardized, multi-dimensional, longitudinal data and biospecimens on consented adult cancer patients, high-risk individuals, and normal controls. The distinct characteristic of the iCaRe2 is its geographical coverage, with a significant percentage of small and …
NCT02089789 — Clinical and Basic Investigations Into Known and Suspected Congenital Disorders of Glycosylation
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Human Genome Research Institute (NHGRI) |
| Enrollment | 200 |
| Study Type | OBSERVATIONAL |
| Conditions | Congenital Disorders of Glycosylation |
Background:
- Proteins, fats, and other molecules are the body s building blocks. Many of these molecules must have sugars, or chains of sugars, attached to work properly. People with congenital disorders of glycosylation (CDGs) cannot attach these sugars or sugar chains properly. A child or adult with a CDG can have symptoms in different parts of the body, including brain, nerves, muscles, l…
NCT03841617 — The Use of 124-I-PET/CT Whole Body and Lesional Dosimetry in Differentiated Thyroid Cancer
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Thyroid Cancer |
| Interventions | ; ; |
Study rationale
High risk patients with differentiated thyroid cancer (DTC) require therapy with 131 I under thyroid stimulating hormone (TSH) stimulation. There are two methods of TSH stimulation endogenous by thyroid hormone withdrawal (THW) leading to hypothyroidism and exogenous by injection of human recombinant TSH (rhTSH Thyrogen). The appropriate 131-I activity utilized for treatment is…
NCT04892303 — Combination Radiotherapy and Radiopharmaceutical Therapy Treatment Planning for Thyroid Cancer
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins |
| Enrollment | 48 |
| Study Type | INTERVENTIONAL |
| Conditions | Recurrent Thyroid Cancer |
| Interventions |
The goal of this study is to evaluate combined radioactive iodine (RAI, 131-I) and external beam radiotherapy (XRT) to optimize the radiation dose delivered to treat well differentiated thyroid cancers (DTC) with iodine-avid metastases. The investigators hypothesize that precise dosimetric planning will permit this combined RAI-XRT radiotherapeutic approach to be safe and permit higher tumor ra…
NCT05355701 — A Study to Learn About the Study Medicine Called PF-07799933 in People With Advanced Solid Tumors With BRAF Alterations.
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Pfizer |
| Enrollment | 267 |
| Study Type | INTERVENTIONAL |
| Conditions | Melanoma; Non-Small-Cell Lung Cancer; Thyroid Cancer; Glioma; Advanced Colorectal Cancer (Part 1) |
| Interventions | ; ; |
The purpose of this clinical trial is to learn about the safety and effects of the study medicine (called PF-07799933) administered as a single agent and in combination with other study medicines in people with solid tumors.
This study is seeking participants who have an advanced solid tumor with a certain type of abnormal gene called “BRAF” and available treatments are no longer effective in …
NCT05334069 — Collecting Blood Samples From Patients With and Without Cancer to Evaluate Tests for Early Cancer Detection
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Alliance for Clinical Trials in Oncology |
| Enrollment | 2000 |
| Study Type | OBSERVATIONAL |
| Conditions | Acute Lymphoblastic Leukemia; Acute Myeloid Leukemia; Ann Arbor Stage I Lymphoma; Ann Arbor Stage II Lymphoma; Ann Arbor Stage III Lymphoma |
| Interventions | ; |
This study collects blood and tissue samples from patients with cancer and without cancer to evaluate tests for early cancer detection. Collecting and storing samples of blood and tissue from patients with and without cancer to study in the laboratory may help researchers develop tests for the early detection of cancers.
NCT05538130 — A Study to Learn About the Study Medicine Called PF-07799544 as Monotherapy or in Combination in People With Advanced Solid Tumors
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Pfizer |
| Enrollment | 124 |
| Study Type | INTERVENTIONAL |
| Conditions | Melanoma; Glioma; Thyroid Cancer; Non-Small Cell Lung Cancer; Malignant Neoplasms |
| Interventions | ; |
The purpose of this clinical trial is to learn the safety and effects of the study medicine (PF-07799544) alone or in combination as a potential cancer treatment for adults with advanced solid tumors. The study will be conducted in two parts: PF-07799544 as a single agent (Phase 1a) and PF-07799544 in combination with another study medicine called PF-07799933 (Phase 1b).
Phase 1a is no longer …
NCT06401044 — A Study of AMG 732 in Healthy Participants and Participants With Thyroid Eye Disease
| Status | Recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | Amgen |
| Enrollment | 88 |
| Study Type | INTERVENTIONAL |
| Conditions | Thyroid Eye Disease |
| Interventions | ; |
The primary objective of Part A of this study is to investigate the safety and tolerability of AMG 732 after single subcutaneous (SC) doses. The primary objective of Part B of this study is to investigate the efficacy of AMG 732 in participants with Thyroid Eye Disease (TED) after multiple SC doses.
NCT06771219 — SLV-154 Treatment of Metastatic Solid Tumors
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Solve Therapeutics |
| Enrollment | 70 |
| Study Type | INTERVENTIONAL |
| Conditions | Squamous Cell Cancer of Head and Neck (SCCHN); NSCLC; SCLC; Cervical Cancer Metastatic; Breast Cancer Metastatic |
| Interventions |
This is a Phase 1 dose-escalation study evaluating the safety, pharmacokinetics, pharmacodynamics, immunogenicity, and efficacy of SLV-154 across a range of dose levels when administered to subjects with metastatic solid tumors.
NCT06959641 — XL092 for the Treatment of Locally Advanced or Metastatic Radioiodine Refractory Differentiated Thyroid Cancer
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Jochen Lorch |
| Enrollment | 33 |
| Study Type | INTERVENTIONAL |
| Conditions | Locally Advanced Differentiated Thyroid Gland Carcinoma; Locally Advanced Poorly Differentiated Thyroid Gland Carcinoma; Locally Advanced Thyroid Gland Follicular Carcinoma; Locally Advanced Thyroid Gland Oncocytic Carcinoma; Locally Advanced Thyroid Gland Papillary Carcinoma |
| Interventions | ; ; |
This phase II trial tests how well XL092 works for the treatment of patients with differentiated thyroid cancer that has not responded to previous treatment with radioiodine (radioiodine refractory) and that has spread to nearby tissue or lymph nodes (locally advanced) or that has spread from where it first started (primary site) to other places in the body (metastatic). XL092 is in a class of …
NCT06984627 — A Study to Investigate the Efficacy and Safety of Rilzabrutinib in Adult Participants With Graves’ Disease
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Sanofi |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Graves’ Disease |
| Interventions | ; |
This is a parallel group, Phase 2, 2-arm study to measure the treatment effect and safety of rilzabrutinib dose 1 or rilzabrutinib dose 2 in participants with Graves’ disease, with and without Graves’ orbitopathy, aged 18 years or older.
Study details include:
- Screening period (up to 4 weeks).
- Treatment period (up to 16 weeks).
- Follow-up period (4 weeks). The number of visits will be up…
NCT07124000 — DESTINY-PANTUMOUR04
| Status | Recruiting |
| Phase | N/A |
| Sponsor | AstraZeneca |
| Enrollment | 100 |
| Study Type | OBSERVATIONAL |
| Conditions | Adenocarcinoma (NOS); Anal Cancer; Bladder Cancer; Cervical Cancer; Endometrial Cancer |
| Interventions |
This study will evaluate the effectiveness of T-DXd in patients with HER2-positive (IHC 3+) locally advanced, unresectable, or metastatic solid tumors who have received prior systemic treatment for metastatic or advanced disease and have no satisfactory alternative treatment options in a real-world setting in the US
NCT07244835 — A Study of DEG6498 in Participants With Solid Tumors
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Degron Therapeutics Co. |
| Enrollment | 100 |
| Study Type | INTERVENTIONAL |
| Conditions | Malignant Neoplasms |
| Interventions |
The goal of this first in human, Phase 1, multi-center, open-label, and 2-part study is to learn whether DEG6498 is safe and tolerable in participants with advanced solid tumors. It will also learn about DEG6498 pharmacokinetics (PK) profile and potential antitumor activity. The main questions it aims to answer are:
- what is an appropriate dose to be given to participants?
- are the side effe…
NCT07288138 — A Study of a Thyroid Hormone Receptor Beta Isoform (THRβ) Agonist and an Semicarbazide Sensitive Amine Oxidase (SSAO) Inhibitor, Alone and in Combination, in Adults With Presumed Metabolic Dysfunction-associated Steatohepatitis (MASH)
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Eccogene |
| Enrollment | 160 |
| Study Type | INTERVENTIONAL |
| Conditions | Metabolic Dysfunction-associated Steatohepatitis |
| Interventions | ; ; |
The primary objective of this trial is to evaluate the dose-dependent and comparative effects of ECC4703 (low and high dose), ECC0509 (low and high dose), and their combination on hepatic fat reduction as assessed by change in magnetic resonance imaging proton density fat fraction (MRI-PDFF) at Week 12.
NCT07305818 — NEXUS Study: A Study to Test Single and Multiple Doses of MER511 Given to Adults With Graves’ Disease
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Merida Biosciences |
| Enrollment | 100 |
| Study Type | INTERVENTIONAL |
| Conditions | Graves Disease |
| Interventions | ; ; |
The purpose of this study is to evaluate how well MER511 is tolerated and what side effects may occur in adults who have Graves’ disease. The study drug will be administered either intravenously (into a vein in the arm) or subcutaneously (under the skin).
Blood tests will be performed to investigate how the body processes the study drug and how the study drug affects the body.
NCT07428057 — Postoperative Hypocalcemia After Thyroidectomy
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Minia University |
| Enrollment | 600 |
| Study Type | OBSERVATIONAL |
| Conditions | Thyroid Nodule; Thyroid Dysfunction; Hypocalcemia; Thyroid Cancer; Postoperative Complications |
This retrospective cohort study investigates predictors of postoperative hypocalcemia following thyroidectomy procedures at Minia University Hospital over a 10-year period (2014-2024). Postthyroidectomy hypocalcemia is one of the most common complications of thyroid surgery, affecting 20-50% of patients. The study aims to identify demographic, clinical, laboratory, and surgical factors associat…
NCT07406087 — Navigation Intervention for Adolescent and Young Adult Cancer Survivors
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Kaiser Permanente |
| Enrollment | 25 |
| Study Type | INTERVENTIONAL |
| Conditions | Breast Cancer; Ovarian Cancer; Cervical Cancer; Testicular Cancer; Colon Rectal Cancer |
| Interventions |
The investigators propose to: 1) Adapt an evidence-based cancer-focused patient navigation (PN) program for the Adolescent and Young Adult (AYA) cancer survivor population; and 2) Plan and conduct an effectiveness-implementation trial of this program within Kaiser Permanente Southern California (KPSC). PLEASE NOTE: This study is awarded in two phases. The UG3 phase has been awarded for the firs…
NCT07438405 — An Open-label, Rollover Trial to Evaluate the Efficacy and Safety of AMG 732 in Participants With Thyroid Eye Disease
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Amgen |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Thyroid Eye Disease |
| Interventions |
The main objective of this trial is to assess the efficacy of AMG 732 in participants with thyroid eye disease (TED) who are defined as primary nonresponders or relapsed during the safety follow-up in the parent trial (NCT06401044).
NCT07570316 — A Study to Assess Efficacy and Safety of Efgartigimod PH20 SC PFS in Adult Participants With Graves’ Disease
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | argenx |
| Enrollment | 230 |
| Study Type | INTERVENTIONAL |
| Conditions | Graves’ Disease; Graves Disease |
| Interventions | ; |
The main purpose of this study is to look at how efgartigimod affects thyroid function in adults with Graves’ Disease (GD). The study will also check whether efgartigimod is safe and well tolerated. It will look at how efgartigimod is distributed and eliminated in the body, how it changes antibody levels, and how the immune system responds to it.
The study consists of a part A double-blinded t…
NCT07596849 — A Study to Assess Efficacy and Safety of Efgartigimod PH20 SC PFS in Adult Participants With Graves’ Disease.
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | argenx |
| Enrollment | 230 |
| Study Type | INTERVENTIONAL |
| Conditions | Graves Disease |
| Interventions | ; |
The main purpose of this study is to look at how efgartigimod affects thyroid function in adults with Graves’ Disease (GD). The study will also check whether efgartigimod is safe and well tolerated. It will look at how efgartigimod is distributed and eliminated in the body, how it changes antibody levels, and how the immune system responds to it.
The study consists of a part A double-blinded t…
NCT07682896 — Evaluation of YB-101 for Safety, Tolerability, Pharmacokinetics, and Efficacy in Graves’ Disease
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Yarrow Bioscience, Inc. |
| Enrollment | 232 |
| Study Type | INTERVENTIONAL |
| Conditions | Graves’ Disease |
| Interventions | ; |
This study is being conducted to look at the effect YB-101 has on thyroid function. This study will also evaluate how safe and well tolerated YB-101 is and how it is distributed through the body.
The study consists of a part 1, blinded treatment period, and a part 2 double-blinded treatment period. Participants will receive YB-101 or Placebo subcutaneously. Participants who participate in Part…
NCT07545837 — Health and Wellness Coaching to Improve Adherence to Healthy Habits and Treatment Plans in Papillary and Follicular Thyroid Cancer Survivors
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Mayo Clinic |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Thyroid Gland Follicular Carcinoma; Thyroid Gland Papillary Carcinoma |
| Interventions | ; ; |
This clinical trial evaluates the impact of a patient-centered health and wellness coaching (HWC) intervention on adherence to treatment plans and healthy lifestyle practices in patients with papillary or follicular thyroid cancer. Treatment for thyroid cancer often involves surgery, radioactive iodine and/or lifelong levothyroxine with regular monitoring of thyroid stimulating hormone levels. …
NCT07661056 — Study to Determine if BHV-1300 is Effective and Safe in Adults With Graves’ Disease
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Biohaven Therapeutics Ltd. |
| Enrollment | 300 |
| Study Type | INTERVENTIONAL |
| Conditions | Graves Disease |
| Interventions | ; |
The purpose of this study is to evaluate the efficacy and safety of BHV-1300 in adult participants with Graves’ disease who are actively hyperthyroid
Active, Not Recruiting
NCT02185560 — Prospective, Non-interventional, Post-authorization Safety Study That Includes All Patients Diagnosed as Unresectable Differentiated Thyroid Carcinoma and Treated With Sorafenib
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Bayer |
| Enrollment | 453 |
| Study Type | OBSERVATIONAL |
| Conditions | Thyroid Carcinoma |
| Interventions |
This is a non-interventional, multi center post-authorization safety study that includes all patients diagnosed as Unresectable Differentiated Thyroid Carcinoma (DTC) and treated with Sorafenib within a certain period. The investigator should have made the choice of treatment (NEXAVAR) according with the Japanese Package Insert prior to enrolling the patient in this study.
The enrollment perio…
NCT02465060 — Targeted Therapy Directed by Genetic Testing in Treating Patients With Advanced Refractory Solid Tumors, Lymphomas, or Multiple Myeloma (The MATCH Screening Trial)
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 6452 |
| Study Type | INTERVENTIONAL |
| Conditions | Advanced Lymphoma; Advanced Malignant Solid Neoplasm; Bladder Carcinoma; Breast Carcinoma; Cervical Carcinoma |
| Interventions | ; ; |
This phase II MATCH screening and multi-sub-trial studies how well treatment that is directed by genetic testing works in patients with solid tumors, lymphomas, or multiple myelomas that may have spread from where it first started to nearby tissue, lymph nodes, or distant parts of the body (advanced) and does not respond to treatment (refractory). Patients must have progressed following at leas…
NCT03085056 — Trametinib in Combination With Paclitaxel in the Treatment of Anaplastic Thyroid Cancer
| Status | Active, not recruiting |
| Phase | Early Phase 1 |
| Sponsor | Memorial Sloan Kettering Cancer Center |
| Enrollment | 13 |
| Study Type | INTERVENTIONAL |
| Conditions | Anaplastic Thyroid Cancer |
| Interventions | ; |
The purpose of this study is to test the safety and tolerability of this treatment combination of paclitaxel and trametinib. Additionally, this study aims to to find out what effects the combination of paclitaxel and trametinib has on the shrinkage and growth of anaplastic thyroid cancer.
NCT03655223 — Early Check: Expanded Screening in Newborns
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | RTI International |
| Enrollment | 30000 |
| Study Type | OBSERVATIONAL |
| Conditions | Spinal Muscular Atrophy; Fragile X Syndrome; Fragile X - Premutation; Duchenne Muscular Dystrophy; Hyperinsulinemic Hypoglycemia, Familial 1 |
| Interventions |
Early Check provides voluntary screening of newborns for a selected panel of conditions. The study has three main objectives: 1) develop and implement an approach to identify affected infants, 2) address the impact on infants and families who screen positive, and 3) evaluate the Early Check program. The Early Check screening will lead to earlier identification of newborns with rare health condi…
NCT04238624 — Study of Cemiplimab Combined With Dabrafenib and Trametinib in People With Anaplastic Thyroid Cancer
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | Memorial Sloan Kettering Cancer Center |
| Enrollment | 16 |
| Study Type | INTERVENTIONAL |
| Conditions | Anaplastic Thyroid Cancer; Thyroid Cancer; BRAF Gene Mutation; BRAF Mutation-Related Tumors |
| Interventions | ; |
This study is being done to see if adding the study drug, cemiplimab, to the standard therapy with dabrafenib and trametinib is an effective treatment against anaplastic thyroid cancer.
NCT04521686 — Study of LY3410738 Administered to Patients With Advanced Solid Tumors With IDH1 or IDH2 Mutations
| Status | Active, not recruiting |
| Phase | Phase 1 |
| Sponsor | Eli Lilly and Company |
| Enrollment | 200 |
| Study Type | INTERVENTIONAL |
| Conditions | Cholangiocarcinoma; Chondrosarcoma; Glioma; Any Solid Tumor |
| Interventions | ; ; |
This is an open-label, multicenter Phase 1 study to evaluate safety, tolerability and preliminary efficacy of oral LY3410738 in patients with isocitrate dehydrogenase 1 (IDH1) arginine 132 (R132)-mutant advanced solid tumors, including but not limited to cholangiocarcinoma, chondrosarcoma, and glioma or isocitrate dehydrogenase 2 (IDH2) arginine 140 (R140) or arginine 172 (R172) mutant cholangi…
NCT04940052 — Study of Efficacy and Safety of Dabrafenib in Combination With Trametinib in Previously Treated Patients With Metastatic, Radio-active Iodine Refractory BRAF V600E Mutation Positive Differentiated Thyroid Cancer
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | Novartis Pharmaceuticals |
| Enrollment | 153 |
| Study Type | INTERVENTIONAL |
| Conditions | Differentiated Thyroid Cancer (DTC) |
| Interventions | ; ; |
The purpose of this study is to assess the efficacy and safety of dabrafenib in combination with trametinib for treating adult patients with locally advanced or metastatic Differentiated Thyroid Cancer (DTC) harboring the BRAFV600E mutation, who are refractory to radioactive iodine (RAI) therapy and have experienced disease progression following one or two prior VEGFR-targeted treatments.
NCT06248619 — A Trial to Investigate Teprotumumab Subcutaneous Administration Compared With Placebo in Male and Female Adult Participants With Moderate-to-severe Active Thyroid Eye Disease
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | Amgen |
| Enrollment | 89 |
| Study Type | INTERVENTIONAL |
| Conditions | Thyroid Eye Disease |
| Interventions | ; |
The study consists of a randomized double-masked, placebo-controlled, parallel-group, multicenter trial with an optional open-label treatment period for proptosis non-responders who complete the Double-masked Treatment Period.
NCT07023731 — A Study to Evaluate ARV-806 in Adults With Advanced Cancer That Has the KRAS G12D Mutation
| Status | Active, not recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | Arvinas Inc. |
| Enrollment | 159 |
| Study Type | INTERVENTIONAL |
| Conditions | KRAS G12D Mutation; Advanced Solid Cancer |
| Interventions |
This is a study to evaluate the safety and potential anti-tumor activity of an investigational agent called ARV-806 in Adults with Advanced Cancer having a specific Kirsten rat sarcoma viral oncogene homolog (KRAS) mutation. This is an open-label study which means that participants and study staff will know that all participants will receive ARV-806.
Researchers think that ARV-806 can work by …
NCT07118176 — Determining the Biodistribution of an Imaging Tracer (68Ga-FAPi-46) in Patients With Solid Tumors or Hematologic Cancers
| Status | Active, not recruiting |
| Phase | Phase 1 |
| Sponsor | Jonsson Comprehensive Cancer Center |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Anal Carcinoma; Bladder Carcinoma; Breast Carcinoma; Cervical Carcinoma; Cholangiocarcinoma |
| Interventions | ; ; |
This phase I trial is evaluating a new imaging tracer (68Ga-FAPi-46) with positron emission tomography (PET)/computed tomography (CT) to determine where and to which degree the tracer (68Ga-FAPi-46) accumulates in normal and cancer tissues (the biodistribution) in patients with solid tumors or hematologic (blood) cancers. PET is an established imaging technique that utilizes small amounts of ra…
Not Yet Recruiting
NCT06991738 — 177Lu-DOTA-EB-TATE in Adult Patients With Metastatic, Radioactive Iodine Non-Responsive Oncocytic (Hurthle-Cell) Thyroid Cancer
| Status | Not yet recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) |
| Enrollment | 18 |
| Study Type | INTERVENTIONAL |
| Conditions | Thyroid Cancer |
| Interventions | ; ; |
Background:
Oncocytic (Hurthle cell) thyroid cancer (HTC) is a rare disease with few treatment options. Researchers are developing a radioactive drug that targets a protein that appears in high numbers on HTC cancer cells.
Objective:
To test a radioactive drug (177LuDOTA-EB-TATE) in people with HTC.
Eligibility:
People aged 18 years and older with HTC. The HTC must have failed to respond t…
NCT07690839 — Pre-Clinic Visit Online Education for Thyroid Cancer
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Cedars-Sinai Medical Center |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Thyroid Cancer |
| Interventions | ; |
Through a pilot randomized controlled trial (RCT), we aim to test the feasibility and preliminary impact of two online educational resources among adult patients with thyroid cancer. Each online program can be accessed on the patient’s personal device, and will be provided to the patient following a diagnosis of thyroid cancer but before meeting with their surgeon to discuss treatment options. …
Completed Trials
NCT01813136 — Phase II Study of the Optimal Scheme of Administration of Pazopanib in Thyroid Carcinoma
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | Centre Leon Berard |
| Enrollment | 168 |
| Study Type | INTERVENTIONAL |
| Conditions | Thyroid Carcinoma |
| Interventions | ; |
The objective of this study is to determine the feasibility of pazopanib treatment interruption with reintroduction at progression in iodine refractory progressive Differentiated Thyroid Cancer (DTC) patients as compared to pazopanib continuous administration.
NCT07681557 — Oxidized Regenerated Cellulose and Voice Quality After Total Thyroidectomy
| Status | Completed |
| Phase | N/A |
| Sponsor | Ankara University |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Thyroid Diseases; Postoperative Voice Change |
| Interventions |
This randomized controlled trial evaluated whether placement of oxidized regenerated cellulose (ORC) over the recurrent laryngeal nerves during total thyroidectomy affects early postoperative voice quality. Patients undergoing bilateral total thyroidectomy for benign or malignant thyroid disease were assigned in a 1:1 ratio to bilateral placement of ORC within the thyroid bed or to conventional…
NCT02576431 — A Study to Test the Effect of the Drug Larotrectinib in Adults and Children With NTRK-fusion Positive Solid Tumors
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | Bayer |
| Enrollment | 215 |
| Study Type | INTERVENTIONAL |
| Conditions | Solid Tumors Harboring NTRK Fusion |
| Interventions |
This research study is done to test how well different types of cancer respond to the drug called larotrectinib. The cancer must have a change in a particular gene (NTRK1, NTRK2 or NTRK3). Larotrectinib is a drug that blocks the actions of these NTRK genes in cancer cells and can therefore be used to treat cancer.
NCT02856347 — Prospective Study Evaluating the Medullary Thyroid Cancer Management’s Care Using PET F-DOPA in Patients With a High Level of Postoperative Residual Thyrocalcitonin
| Status | Completed |
| Phase | N/A |
| Sponsor | Institut Claudius Regaud |
| Enrollment | 24 |
| Study Type | INTERVENTIONAL |
| Conditions | Medullary Thyroid Cancer |
| Interventions |
The aim of the trial is to study a radiating diagnosis agent used in post surgery when the biological assessment highlighted a residual disease.
This is an inter-regional multicentric, prospective study evaluating the benefit of PET F-DOPA imaging in involved node detection compared to standard imaging assessment in patient with medullary thyroid cancer.
The purpose of the study is to evaluat…
NCT03345563 — Project HERO: Health Empowerment & Recovery Outcomes
| Status | Completed |
| Phase | N/A |
| Sponsor | Rutgers, The State University of New Jersey |
| Enrollment | 113 |
| Study Type | INTERVENTIONAL |
| Conditions | Prostate Cancer; Bladder Cancer; Kidney Cancer; Colon Cancer; Rectum Cancer |
| Interventions | ; ; |
Project HERO is a 12-week study of the efficacy of Body Mind Training (BMT, i.e. Tai Chi and Qigong in this project) for reducing fatigue in male cancer survivors. This 3-arm randomized clinical trial will examine inflammatory biology and selected gene-expression pathways that are hypothesized to contribute to the intervention’s effect.
NCT03986437 — A Prospective Study to Collect Images in Patients Treated With Iodine-131 as Part of a European Research Project in Radiation Protection.
| Status | Completed |
| Phase | N/A |
| Sponsor | Institut Claudius Regaud |
| Enrollment | 29 |
| Study Type | OBSERVATIONAL |
| Conditions | Differentiated Thyroid Cancer |
This trial is a prospective, non-interventional, monocentric study aiming to collect standard of care imaging of patients treated with Iodine-131 for the determination of dosimetric studies.
Data from this study will be collected as part of an European research project called MEDIRAD.
The overall objectives of this project are to enhance the scientific bases and clinical practice of radiation…
NCT04000880 — Adapting Multiple Behavior Interventions That Effectively Improve Cancer Survivor Health Cancer Survivor Health
| Status | Completed |
| Phase | N/A |
| Sponsor | University of Alabama at Birmingham |
| Enrollment | 603 |
| Study Type | INTERVENTIONAL |
| Conditions | Breast Cancer; Colorectal Cancer; Endometrial Cancer; Kidney Cancer; Multiple Myeloma |
| Interventions | ; ; |
This research study will test the efficacy of interactive, web-based interventions that improve diet, physical activity and weight management changes among early stage survivors of breast, prostate, colorectal, endometrial, renal, thyroid, and ovarian cancers, as well as multiple myeloma and non-Hodgkin Lymphoma. Overarching outcomes also include physical function and performance, muscle mass, …
NCT07683039 — Thyroid Fine Needle Biopsy and Impact on Pain and Diagnostic Adequacy
| Status | Completed |
| Phase | N/A |
| Sponsor | Izmir Ataturk Training and Research Hospital |
| Enrollment | 169 |
| Study Type | INTERVENTIONAL |
| Conditions | Thyroid Nodular Disease |
| Interventions | ; |
This randomized study compares patient pain and comfort during ultrasound-guided thyroid fine needle biopsy using 21-gauge versus 27-gauge needles. Patients with thyroid nodules were randomly assigned to one of two needle sizes. Pain intensity was measured immediately after the procedure using a 0-100 Visual Analog Scale. The study was conducted at İzmir Atatürk Training and Research Hospital b…
NCT07652450 — Incidental Thyroid Cancer in Cases With Inflammatory Thyroid Lesion
| Status | Completed |
| Phase | N/A |
| Sponsor | Minia University |
| Enrollment | 200 |
| Study Type | INTERVENTIONAL |
| Conditions | Papillary Thyroid Cancer; Hashimoto Disease; Hashimoto's Thyroiditis; Follicular Thyroid Cancer |
| Interventions |
This study aim to assess for the incidence of thyroid cancer in patients with autoimmune thyroiditis (Inflammatory thyroid Lesions)
NCT07688824 — The Effect of SPU on Hormonal and Cardiometabolic Factors
| Status | Completed |
| Phase | N/A |
| Sponsor | King Abdullah University Hospital |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Hypothyroidism; Hypertension; Healthy Adult; Diabete Mellitus; Hyperthyroidism |
| Interventions |
The study examines the immediate effect of soleus pushup exercise on cardiometabolic and hormonal functions among hypothyroid patients.
Other (Terminated)
NCT05228184 — Use of Tirosint®-SOL or Tablet Formulations of Levothyroxine in Pediatric Patients With Congenital Hypothyroidism (CH)
| Status | Terminated |
| Phase | Phase 4 |
| Sponsor | IBSA Institut Biochimique SA |
| Enrollment | 34 |
| Study Type | INTERVENTIONAL |
| Conditions | Congenital Hypothyroidism |
| Interventions | ; |
This is a multi-center, prospective, parallel-group, open-label, randomized clinical study in one hundred and twenty-six (126) neonates and infants diagnosed with CH.
Subjects will be randomized in a 2:1 ratio to Treatment (Tirosint®-SOL) or Control (conventional therapy with levothyroxine sodium crushed tablets).