Clinical Trials on Crouzon Syndrome

Total 36 results

    • NCT03773302
      Recruiting
      Conditions: Advanced Cholangiocarcinoma; FGFR2 Gene Mutation
    • NCT04093362
      Not yet recruiting
      Conditions: Advanced Cholangiocarcinoma; FGFR2 Gene Rearrangements
    • NCT02150967
      Recruiting
      Conditions: Advanced Cholangiocarcinoma; FGFR2 Gene Mutation
    • NCT04507503
      Available
      Conditions: Advanced Cholangiocarcinoma
    • NCT03230318
      Recruiting
      Conditions: Intrahepatic Cholangiocarcinoma; Combined Hepatocellular and Cholangiocarcinoma
    • NCT02368951
      Terminated
      Conditions: Medical Oncology
    • NCT04479904
      Not yet recruiting
      Conditions: Intrahepatic Cholangiocarcinoma
    • NCT01752920
      Completed
      Conditions: Solid Tumor
    • NCT01719549
      Completed
      Conditions: Gastric Cancer
    • NCT04526106
      Recruiting
      Conditions: Solid Tumor, Adult; FGFR2 Amplification; FGFR2 Gene Mutation; FGFR2 Gene Rearrangement; FGFR2 Gene Translocation; FGFR2 Gene Activation; Intrahepatic Cholangiocarcinoma; Cholangiocarcinoma; Endometrial Cancer; Gastric Cancer; Breast Cancer
    • NCT04096417
      Recruiting
      Conditions: FGFR1 Gene Amplification; FGFR1 Gene Mutation; FGFR1 Gene Translocation; FGFR2 Gene Amplification; FGFR2 Gene Mutation; FGFR2 Gene Translocation; FGFR3 Gene Amplification; FGFR3 Gene Mutation; FGFR3 Gene Translocation; Metastatic Colorectal Carcinoma; Stage III Colorectal Cancer AJCC v8; Stage IIIA Colorectal Cancer AJCC v8; Stage IIIB Colorectal Cancer AJCC v8; Stage IIIC Colorectal Cancer AJCC v8; Stage IV Colorectal Cancer AJCC v8; Stage IVA Colorectal Cancer AJCC v8; Stage IVB Colorectal Cancer AJCC v8; Stage IVC Colorectal Cancer AJCC v8; Unresectable Colorectal Carcinoma
    • NCT02965378
      Active, not recruiting
      Conditions: FGFR1 Gene Amplification; FGFR1 Gene Mutation; FGFR2 Gene Amplification; FGFR2 Gene Mutation; FGFR3 Gene Amplification; FGFR3 Gene Mutation; Recurrent Squamous Cell Lung Carcinoma; Stage IV Squamous Cell Lung Carcinoma AJCC v7
    • NCT02706691
      Terminated
      Conditions: FGFR Gene Amplification; FGFR1 Gene Amplification; FGFR2 Gene Amplification; FGFR2 Gene Mutation; FGFR3 Gene Mutation; Head and Neck Squamous Cell Carcinoma; Human Papillomavirus Infection; Recurrent Head and Neck Carcinoma; Recurrent Nasopharynx Carcinoma; Recurrent Oropharyngeal Squamous Cell Carcinoma
    • NCT01144741
      Recruiting
      Conditions: Freeman-Sheldon Syndrome; Arthrogryposis Distal Type 2A; Whistling Face Syndrome; Craniocarpotarsal Dysplasia; Craniocarpotarsal Dystrophy; Freeman-Sheldon Syndrome Variant; Sheldon-Hall Syndrome; Arthrogryposis Distal Type 2B; Gordon Syndrome; Arthrogryposis Distal Type 3; Arthrogryposis Distal Type 1; Arthrogryposis, Distal, Type 1A; Arthrogryposis Distal Type 1B; Arthrogryposis, Distal; Craniofacial Abnormalities; Arthrogryposis
    • NCT02052778
      Active, not recruiting
      Conditions: Cholangiocarcinoma; Brain Tumor; Urothelial Cancer; Other Tumor Types With FGFR2 Gene Fusions; Activating Mutations; FGFR2 Amplification
    • NCT04238715
      Recruiting
      Conditions: Cholangiocarcinoma
    • NCT01630460
      Recruiting
      Conditions: Craniometaphyseal Dysplasia
    • NCT04056858
      Completed
      Conditions: Goldenhar Syndrome; Oculoauriculovertebral Dysplasia
    • NCT04351893
      Recruiting
      Conditions: Microtia; Microtia-Anotia; Craniofacial Microsomia; Goldenhar Syndrome; OAVS; OAV Syndrome; Hemifacial Microsomia
    • NCT03869021
      Completed
      Conditions: Hemifacial Microsomia
    • NCT03861650
      Completed
      Conditions: Hemifacial Microsomia; Distraction of Bone
    • NCT03806361
      Active, not recruiting
      Conditions: Craniofacial Microsomia
    • NCT03720990
      Not yet recruiting
      Conditions: Smith-Lemli-Opitz Syndrome
    • NCT02494752
      Unknown status
      Conditions: Romberg's Disease; Craniofacial Microsomia; Lipodystrophy; Mixed Connective Tissue Disease
    • NCT02224677
      Unknown status
      Conditions: Craniofacial Microsomia; Hemifacial Microsomia; Oculo-Auriculo-Vertebral-Syndrome; Goldenhar Syndrome; Microtia