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Neoplastic Syndromes, Hereditary

Clinical trial condition

Neoplastic Syndromes, Hereditary

Explore clinical trials studying Neoplastic Syndromes, Hereditary. Study availability and eligibility vary by location and protocol.

869 public trials 154 recruiting studies

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Neoplastic Syndromes, Hereditary trial results

Completed

Biomarkers in Samples From Younger Patients With Wilms Tumor

NCT01493817

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, +15 more
Locations: Children's Oncology Group Monrovia, California, United States

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Completed

Gene Expression Profiles to Categorize Wilms Tumors

NCT00897637

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, +20 more
Locations: Children's Oncology Group Arcadia, California, United States

Saint Mary's Hospital West Palm Beach, Florida, United States

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Completed

Studying Biomarkers in Samples From Younger Patients With Wilms Tumor

NCT01542333

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, +15 more
Locations: Not specified

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Completed

Biomarkers in Blood and Tumor Tissue Samples From Patients With Wilms Tumor

NCT01314391

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, +17 more
Locations: Not specified

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Completed

Studying Genes Using Cord Blood and Placenta Samples From Relatively Healthy Newborns and Samples From Younger Patients With Wilms Tumor

NCT01576211

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, +15 more
Locations: Not specified

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Completed

Chromoendoscopy to Decrease the Risk of Colorectal Neoplasia in Lynch Syndrome

NCT00905710

Conditions: Colonic Diseases, Colorectal Neoplasms, Colorectal Neoplasms, Hereditary Nonpolyposis, +16 more
Locations: University Medical Center Groningen Groningen, Netherlands

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Completed

Maintenance of Muscle Mass in Older People: the Negative Impact of Statin Therapy

NCT01047163

Conditions: Atrophy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Endocrine Gland Neoplasms, +22 more
Locations: David Greenfield Physiology Laboratories Nottingham, Nottinghamshire, United Kingdom

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Completed

Phase II Study of Gleevec/Imatinib Mesylate (STI-571, NCS 716051) in Neurofibromatosis (NF1) Patients With Plexiform Neurofibromas

NCT01673009

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +11 more
Locations: Indiana University Indianapolis, Indiana, United States

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Completed

Prognostic Role of Minimal Residual Disease in Acute Myeloid Leukemia

NCT02714790

Conditions: Acute Myeloid Leukemia, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Female Urogenital Diseases, +25 more
Locations: Not specified

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Completed

Lapatinib Study for Children and Adults With Neurofibromatosis Type 2 (NF2) and NF2-Related Tumors

NCT00973739

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cranial Nerve Diseases, Cranial Nerve Neoplasms, +28 more
Locations: New York University School of Medicine New York, United States

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Neoplastic Syndromes, Hereditary

Neoplastic Syndromes, Hereditary trial results

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