- Trials with a EudraCT protocol (50)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
50 result(s) found for: Anterior pituitary.
Displaying page 1 of 3.
EudraCT Number: 2009-010918-30 | Sponsor Protocol Number: 2377 | Start Date*: 2009-08-11 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Amar Agha, Beaumont Hospital | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Effect of growth hormone replacement on cortisol-to-cortisone interconversion in hypopituitary patients with growth hormone deficiency and the influence of different aetiologies of hypopituitarism. | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: 20 patients with hypopituitarism including growth hormone deficiency will be evaluated both on growth hormone replacement and when they have been off it for a 2 month period. They will have been pr... | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: IE (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005018-37 | Sponsor Protocol Number: | Start Date*: 2008-01-18 | |||||||||||||||||||||
Sponsor Name:Amar Agha | |||||||||||||||||||||||
Full Title: Optimal glucocorticoid replacement therapy in adrenocorticotropin (ACTH) deficient hypopituitary patients | |||||||||||||||||||||||
Medical condition: 10 male patients with hypopituitarism resulting in ACTH (adrenocorticotropin) deficiency (ICD E23.0) will be studied on varying doses of hydrocortisone replacement therapy. THis is not a new medica... | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||||||||||||
Trial protocol: IE (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001183-30 | Sponsor Protocol Number: D539OL00074 | Start Date*: 2012-03-09 | |||||||||||
Sponsor Name:Nemours Children's Clinic | |||||||||||||
Full Title: Double-blind trial investigating the safety and efficacy of the inhibitor anastrozole (arimidex) in delaying epiphyseal fusion and increasing height potential of adolescent males with growth hormon... | |||||||||||||
Medical condition: hypopituitarism | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000056-14 | Sponsor Protocol Number: 06/DTD/3791E | Start Date*: 2008-03-03 | ||||||||||||||||
Sponsor Name:Cardiff University | ||||||||||||||||||
Full Title: Determination of method-specific normal cortisol and adrenal hormone responses to the short Synacthen test | ||||||||||||||||||
Medical condition: Normal, healthy volunteers to establish a reference range for the synacthen test, plus patients with hypoadrenalism/hypopituitarism | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-020679-21 | Sponsor Protocol Number: CS/München 02 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Max-Planck-Institut für Psychiatrie | |||||||||||||
Full Title: Growth hormone and gonadotropin deficiency after brain injury (traumatic brain injury, subarachnoidal hemorrhage, ischemic stroke): the effects of hormone replacement on cognition,quality of life a... | |||||||||||||
Medical condition: hormonal deficiency after traumatic brain injury, subarachnoidal hemorrhage and ischemic stroke) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001915-35 | Sponsor Protocol Number: 08052017 | Start Date*: 2017-09-15 |
Sponsor Name:Medical University of Graz | ||
Full Title: GLUCOCORTICOID HIGH-DOSE VS. REPLACEMENT IN IMMUNE CHECKPOINT INHIBITOR ASSOCIATED HYPOPHYSITIS: AN OPEN, RANDOMIZED PILOT STUDY | ||
Medical condition: Immune regulatory antibodies (e.g. ipilimumab, pembrolizumab and nivolumab) inhibiting immunological checkpoints are increasingly used to treat various oncological entities. Potential side effects ... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-003327-23 | Sponsor Protocol Number: IP107-001 | Start Date*: 2008-10-29 | |||||||||||
Sponsor Name:Endo Pharmaceuticals Solutions Inc | |||||||||||||
Full Title: PHASE III, OPEN-LABEL, MULTICENTER INTERNATIONAL STUDY TO EVALUATE THE EFFICACY AND SAFETY OF AN OCTREOTIDE IMPLANT VERSUS SANDOSTATIN LAR® DEPOT IN PATIENTS WITH ACROMEGALY | |||||||||||||
Medical condition: Acromegaly | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) CZ (Completed) PL (Completed) DE (Completed) ES (Completed) SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001972-36 | Sponsor Protocol Number: CSOM230C2305 | Start Date*: 2007-11-15 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A multicenter, randomized, blinded study to assess the safety and efficacy of pasireotide LAR vs. octreotide LAR in patients with active acromegaly. | |||||||||||||
Medical condition: Acromegaly is characterized by chronic hypersecretion of growth hormone (GH), clinical features comprise structural and functional changes occurring in practically all organs. Cardiovascular diseas... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) FR (Completed) BE (Completed) GB (Completed) GR (Completed) IT (Completed) ES (Completed) NL (Completed) DK (Completed) SE (Completed) HU (Completed) PL (Completed) PT (Prematurely Ended) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000737-31 | Sponsor Protocol Number: OOC-ACM-303 | Start Date*: 2017-10-27 | |||||||||||
Sponsor Name:Chiasma, Inc. | |||||||||||||
Full Title: A phase 3, randomized, double-blind, placebo-controlled, multicenter study to evaluate efficacy and safety of octreotide capsules in patients who previously tolerated and demonstrated biochemical c... | |||||||||||||
Medical condition: Acromegaly | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) HU (Completed) NL (Completed) SE (Completed) DK (Completed) PL (Completed) IT (Completed) BG (Completed) LV (Completed) SI (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000675-20 | Sponsor Protocol Number: ISIS766720-CS5 | Start Date*: 2020-11-04 | |||||||||||
Sponsor Name:Ionis Pharmaceuticals, Inc. | |||||||||||||
Full Title: An Open Label, Randomized, Phase 2 Study to Assess the Safety, Tolerability, and Efficacy of IONIS GHR-LRX, an Antisense Inhibitor of the Growth Hormone Receptor, Administered Monthly as Monotherap... | |||||||||||||
Medical condition: Acromegaly is a chronic disorder caused by GH hypersecretion, most commonly as a result of a GH-secreting pituitary adenoma. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) LT (Completed) PL (Completed) LV (Prematurely Ended) IT (Completed) RO (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000155-34 | Sponsor Protocol Number: 2 79 52030 207 | Start Date*: 2008-06-02 | |||||||||||
Sponsor Name:Beaufour Ipsen Pharma | |||||||||||||
Full Title: PHASE IIIb, MULTICENTRE, OPEN-LABEL, SINGLE-ARM, STUDY TO ASSESS THE EFFICACY AND SAFETY OF LANREOTIDE AUTOGEL 120 mg ADMINISTERED EVERY 28 DAYS AS PRIMARY MEDICAL TREATMENT IN ACROMEGALIC PATIENTS... | |||||||||||||
Medical condition: ACROMEGALY ASSOCIATED WITH PITUITARY GLAND MACROADENOMA | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) FR (Completed) ES (Prematurely Ended) SE (Completed) GB (Completed) BE (Completed) CZ (Completed) FI (Completed) DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004386-24 | Sponsor Protocol Number: PEGACRO | Start Date*: 2015-12-04 | |||||||||||
Sponsor Name:DIPARTIMENTO DI MEDICINA CLINICA E CHIRURGIA - UNIVERSITÀ DEGLI STUDI DI NAPOLI FEDERICO II | |||||||||||||
Full Title: Effect of GH receptor antagonist on insulin resistance associated with acromegaly | |||||||||||||
Medical condition: acromegaly | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002849-12 | Sponsor Protocol Number: CSOM230B2201E1 | Start Date*: 2005-01-12 | |||||||||||
Sponsor Name:Novartis Pharmaceuticals UK Ltd | |||||||||||||
Full Title: Extension to a multicenter, randomized, crossover, open label, dose finding study to compare the safety, efficacy and PK/PD relationship of multiple doses of SOM230 (200, 400 and 600 µg b.i.d.) and... | |||||||||||||
Medical condition: Acromegaly is a rare, serious condition characterized by chronic hypersecretion of GH (growth hormone) caused in over 95% of patients by a GH-secreting pituitary adenoma. Clinical manifestations ar... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005431-70 | Sponsor Protocol Number: CRN00808-09 | Start Date*: 2022-03-04 | |||||||||||
Sponsor Name:Crinetics Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Randomized, Controlled, Multi-Center Study to Evaluate the Safety and Efficacy of Paltusotine in Subjects with Acromegaly Treated with Long-acting Somatostatin Receptor Ligands | |||||||||||||
Medical condition: Acromegaly | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Trial now transitioned) AT (Completed) DE (Completed) HU (Trial now transitioned) PL (Trial now transitioned) BG (Trial now transitioned) ES (Completed) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-001703-32 | Sponsor Protocol Number: CRN00808-08 | Start Date*: 2022-03-29 | |||||||||||
Sponsor Name:Crinetics Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Randomized, Controlled, Multicenter Study to Evaluate the Safety and Efficacy of Paltusotine in Subjects with Non-pharmacologically Treated Acromegaly | |||||||||||||
Medical condition: Acromegaly | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Trial now transitioned) PL (Trial now transitioned) ES (Ongoing) IT (Trial now transitioned) GR (Trial now transitioned) BG (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005585-12 | Sponsor Protocol Number: 1 | Start Date*: 2007-12-20 | |||||||||||
Sponsor Name:Department of Internal Medicine of the University of Munich | |||||||||||||
Full Title: Prospektive, offene Studie zur Prüfung der Wirksamkeit der zusätzlichen Gabe des Somatostatinanalogon Octreotid (Sandostatin) bzw. des Dopaminagonisten Cabergolin (Dostinex) bei Patientin mit Akrom... | |||||||||||||
Medical condition: acromegaly (= growth hormone hypersecretion mostly caused by a pituitary adenoma) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016722-13 | Sponsor Protocol Number: CSOM230C2402 | Start Date*: 2010-06-10 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A phase III, multicenter, randomized, parallel-group study to assess the efficacy and safety of double-blind pasireotide LAR 40 mg and pasireotide LAR 60 mg versus open-label octreotide LAR or lanr... | |||||||||||||
Medical condition: Acromegaly is characterized by chronic hypersecretion of growth hormone (GH), clinical features comprise structural and functional changes occurring in practically all organs. Cardiovascular diseas... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) ES (Completed) IT (Completed) NO (Completed) BE (Completed) DE (Completed) PL (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005852-42 | Sponsor Protocol Number: CSMS995BIC03 | Start Date*: 2007-04-20 | |||||||||||
Sponsor Name:NOVARTIS FARMA | |||||||||||||
Full Title: An open-label, two-step, multicenter European study to evaluate the efficacy and safety of Sandostatin LAR at High Dose or in combination either with GH-receptor antagonist or dopamine-agonist i... | |||||||||||||
Medical condition: acromegaly | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) BE (Completed) PT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004320-21 | Sponsor Protocol Number: C2L-OCT-01 PR-302 | Start Date*: 2007-10-29 | |||||||||||
Sponsor Name:Ambrilia Biopharma Inc. | |||||||||||||
Full Title: OPEN LABEL EXTENSION STUDY EVALUATING THE SAFETY AND BIOLOGICAL ACTIVITY OF A NEW PROLONGED RELEASE FORMULATION OF OCTREOTIDE ACETATE, C2L-OCT-01 PR, ADMINISTERED INTRA MUSCULARLY EVERY 6 WEEKS IN ... | |||||||||||||
Medical condition: Acromegaly | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) SK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002912-10 | Sponsor Protocol Number: CH-ACM-01 | Start Date*: 2011-08-31 | |||||||||||
Sponsor Name:Chiasma, Inc. | |||||||||||||
Full Title: EFFICACY AND SAFETY OF ORAL OCTREOLIN™ IN PATIENTS WITH ACROMEGALY WHO ARE CURRENTLY RECEIVING PARENTERAL SOMATOSTATIN ANALOGS | |||||||||||||
Medical condition: Acromegaly | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) NL (Completed) GB (Completed) DE (Completed) SK (Completed) PL (Completed) IT (Completed) SI (Completed) LT (Completed) | |||||||||||||
Trial results: View results |
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