- Trials with a EudraCT protocol (95)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (29)
95 result(s) found for: Dacarbazine.
Displaying page 1 of 5.
| EudraCT Number: 2013-003545-41 | Sponsor Protocol Number: D1344C00001 | Start Date*: 2014-04-14 | |||||||||||
| Sponsor Name:AstraZeneca AB | |||||||||||||
| Full Title: A Randomised, Double-Blind Study to Assess the Efficacy of Selumetinib (AZD6244, Hyd-Sulfate) in Combination with Dacarbazine Compared with Placebo in Combination with Dacarbazine as First Systemic... | |||||||||||||
| Medical condition: Metastatic uveal melanoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) GB (Completed) CZ (Completed) DE (Completed) NL (Completed) FI (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-005737-11 | Sponsor Protocol Number: PH-L19IL2 DTIC - 03/07 | Start Date*: 2008-01-17 | |||||||||||
| Sponsor Name:PHILOGEN S.P.A. | |||||||||||||
| Full Title: Dose definition and activity evaluation study of the tumor-targeting human L19IL2 monoclonal antibody-cytokine fusion protein in combination with Dacarbazine in patients with metastatic melanoma | |||||||||||||
| Medical condition: unresectable metastatic (stage IV)non-uveal melanoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) DE (Prematurely Ended) AT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2005-006082-14 | Sponsor Protocol Number: CA184024 | Start Date*: 2006-08-03 |
| Sponsor Name:Bristol-Myers Squibb International Corporation | ||
| Full Title: A Multi-Center, Randomized, Double-Blind, Two-Arm, Phase III Study in Patients with Untreated Stage III (Unresectable) or IV Melanoma Receiving Dacarbazine Plus 10 mg/kg of Ipilimumab (MDX-010) vs.... | ||
| Medical condition: Stage III (Unresectable) or IV Melanoma | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NO (Completed) IE (Completed) BE (Completed) HU (Completed) ES (Completed) PT (Completed) DE (Completed) GB (Completed) CZ (Completed) AT (Completed) IT (Completed) NL (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-003718-16 | Sponsor Protocol Number: CA209-066 | Start Date*: 2013-04-04 | |||||||||||
| Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
| Full Title: A Phase 3, Randomized, Double-Blind Study of BMS-936558 vs Dacarbazine in Subjects with Previously Untreated Unresectable or Metastatic Melanoma Country specific Protocol Amendment 05, dated 09-... | |||||||||||||
| Medical condition: Melanoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) FI (Completed) SE (Completed) ES (Completed) DK (Completed) NO (Completed) IT (Completed) PL (Completed) GR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2004-000725-30 | Sponsor Protocol Number: BAY 43-9006/11538 | Start Date*: 2007-11-07 | |||||||||||
| Sponsor Name:Bayer HealthCare AG | |||||||||||||
| Full Title: A phase II, multi-centre, open-label, uncontrolled study to evaluate the efficacy and safety of BAY 43-9006 given daily in combination with repeated 21-day cycles of dacarbazine (DTIC) chemotherapy... | |||||||||||||
| Medical condition: Subjects with advanced, metastatic, histologically confirmed melanoma, for whom treatment with dacarbazine is considered medically acceptable. Subjects should have measurable and evaluable disease ... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2004-002130-18 | Sponsor Protocol Number: C1034T02 | Start Date*: 2007-02-19 | |||||||||||
| Sponsor Name:Centocor B.V. | |||||||||||||
| Full Title: A Phase 1/2 , Multi-Center, Blinded, Randomized, Controlled Study of the Safety and Efficacy of the Human Monoclonal Antibody to Human av Integrins (CNTO 95), Alone and in Combination with Dacarbaz... | |||||||||||||
| Medical condition: Malignant Melanoma Stage IV | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) DE (Prematurely Ended) AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-007265-20 | Sponsor Protocol Number: IPH1101-205 | Start Date*: 2008-03-06 | |||||||||||
| Sponsor Name:Innate Pharma | |||||||||||||
| Full Title: A Phase II open label randomized parallel group non comparative trial to assess efficacy and safety of the association of IPH1101 and IL-2 alone and in combination with dacarbazine, in patients wit... | |||||||||||||
| Medical condition: metastatic melanoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) BE (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-005538-20 | Sponsor Protocol Number: BA2011/15/02 | Start Date*: 2012-05-15 | |||||||||||||||||||||
| Sponsor Name:BioAlliance Pharma | |||||||||||||||||||||||
| Full Title: SAFETY AND EFFICACY OF INTRAMUSCULAR ELECTROTRANSFER OF PLASMID AMEP IN PATIENTS SUFFERING FROM ADVANCED OR METASTATIC MELANOMA: AN OPEN-LABEL PHASE I/II CLINICAL TRIAL THE AIMM STUDY (AMEP IN MET... | |||||||||||||||||||||||
| Medical condition: Treatment of patients suffering from advanced or metastatic melanoma (stages III, IV) | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: SI (Prematurely Ended) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2005-001161-34 | Sponsor Protocol Number: APL-B-016-05 | Start Date*: 2005-10-03 | |||||||||||
| Sponsor Name:Pharma Mar SA | |||||||||||||
| Full Title: Phase I-II multicenter, randomized, open-label, clinical and pharmacokinetic study of plitidepsin, administered alone or in combination with dacarbazine, as front-line therapy to subjects with unre... | |||||||||||||
| Medical condition: unresectable advanced melanoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-012293-12 | Sponsor Protocol Number: NO25026 | Start Date*: 2010-01-25 | |||||||||||
| Sponsor Name:F. Hoffmann-La Roche Ltd. | |||||||||||||
| Full Title: BRIM 3: A Randomized, Open-label, Controlled, Multicenter, Phase III Study in Previously untreated Patients with Unresectable Stage IIIC or Stage IV Melanoma with V600E BRAF mutation Receiving Vemu... | |||||||||||||
| Medical condition: First-line therapy for adult patients with histologically confirmed metastatic melanoma (unresectable Stage IIIC or Stage IV) harbouring the V600E positive mutation | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) DE (Completed) FR (Completed) SE (Completed) IT (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-006713-16 | Sponsor Protocol Number: CP12-0604 | Start Date*: 2008-09-02 | |||||||||||
| Sponsor Name:ImClone Systems Incorporated | |||||||||||||
| Full Title: Phase II Randomized, Open-Label Study of IMC-1121B With or Without Dacarbazine in Patients with Metastatic Malignant Melanoma | |||||||||||||
| Medical condition: Metastatic Malignant Melanoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-001828-35 | Sponsor Protocol Number: CA209-037 | Start Date*: 2013-02-15 | |||||||||||
| Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
| Full Title: A Randomized Open-Label Phase III Trial of BMS-936558 versus Investigator’s Choice in Advanced (Unresectable or Metastatic) Melanoma Patients Progressing Post Anti-CTLA-4 Therapy Pharmacogenetic... | |||||||||||||
| Medical condition: Unresectable or metastatic melanoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) NL (Completed) AT (Completed) GB (GB - no longer in EU/EEA) DE (Completed) ES (Completed) IT (Completed) DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-006344-19 | Sponsor Protocol Number: D1532C00006 | Start Date*: 2009-09-03 | |||||||||||||||||||||||||||||||
| Sponsor Name:AstraZeneca AB | |||||||||||||||||||||||||||||||||
| Full Title: A Phase II, Double-Blind, Randomised Study to Assess the Efficacy of AZD6244 (Hyd-Sulfate) in Combination with Dacarbazine Compared with Dacarbazine Alone in First Line Patients with BRAF Mutation ... | |||||||||||||||||||||||||||||||||
| Medical condition: BRAF mutation positive advanced cutaneous and unknown primary melanoma | |||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: DE (Completed) GB (Completed) CZ (Completed) FR (Completed) SE (Completed) HU (Completed) ES (Completed) NL (Completed) | |||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2012-002669-37 | Sponsor Protocol Number: EMR200066-007 | Start Date*: 2013-02-20 | |||||||||||
| Sponsor Name:Merck Serono S.A. Geneva | |||||||||||||
| Full Title: A multicentre, open label, randomized Phase II trial of the MEK inhibitor pimasertib or dacarbazine in previously untreated subjects with N-Ras mutated locally advanced or metastatic malignant cuta... | |||||||||||||
| Medical condition: N-RAS mutated locally advanced or metastatic malignant cutaneous melanoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) GB (Completed) DE (Completed) BE (Completed) ES (Completed) SE (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-004027-17 | Sponsor Protocol Number: SGN35-027 | Start Date*: 2021-09-23 | |||||||||||
| Sponsor Name:Seagen Inc. | |||||||||||||
| Full Title: Multiple Part Clinical Trial of Brentuximab Vedotin in Classical Hodgkin Lymphoma Subjects | |||||||||||||
| Medical condition: Classical Hodgkin Lymphoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Trial now transitioned) PL (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-003593-51 | Sponsor Protocol Number: CMEK162A2301 | Start Date*: 2013-03-27 | |||||||||||
| Sponsor Name:Array BioPharma Inc. | |||||||||||||
| Full Title: The NEMO trial (NRAS melanoma and MEK inhibitor): A randomized Phase III, open label, multicenter, two-arm study comparing MEK162 versus dacarbazine in patients with advanced unresectable or metast... | |||||||||||||
| Medical condition: metastatic or unresectable cutaneous melanoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SK (Completed) AT (Completed) CZ (Completed) DE (Completed) ES (Completed) GB (Completed) NL (Completed) BE (Completed) IT (Completed) HU (Completed) GR (Completed) SE (Completed) PL (Completed) PT (Completed) FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-004097-32 | Sponsor Protocol Number: CA033 | Start Date*: 2009-07-30 | ||||||||||||||||
| Sponsor Name:Abraxis BioScience, LLC, a wholly owned subsidiary of Celgene Corporation | ||||||||||||||||||
| Full Title: An Open-Label, Multicenter, Phase III Trial of ABI-007 vs Dacarbazine in Previously Untreated Patients with Metastatic Malignant Melanoma | ||||||||||||||||||
| Medical condition: Metastatic Malignant Melanoma | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) DE (Completed) NL (Completed) FR (Completed) ES (Completed) IT (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2008-008794-55 | Sponsor Protocol Number: RDD299 | Start Date*: 2010-05-17 | |||||||||||
| Sponsor Name:The Clatterbridge Cancer Centre NHS Foundation Trust | |||||||||||||
| Full Title: A randomised phase II study of sunitinib versus dacarbazine in the treatment of patients with metastatic uveal melanoma | |||||||||||||
| Medical condition: Metastatic Uveal Melanoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-024483-17 | Sponsor Protocol Number: E7389-G000-309 | Start Date*: 2011-06-30 | |||||||||||
| Sponsor Name:Eisai Ltd | |||||||||||||
| Full Title: A Randomised, Open-label, Multicenter, Phase 3 Study to Compare the Efficacy and Safety of Eribulin with Dacarbazine in Subjects with Soft Tissue Sarcoma. | |||||||||||||
| Medical condition: Soft tissue sarcoma (STS) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) DE (Completed) CZ (Completed) GB (Completed) AT (Completed) DK (Completed) ES (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-004103-40 | Sponsor Protocol Number: ALDOXORUBICIN-P3-STS-01 | Start Date*: 2014-03-20 | |||||||||||
| Sponsor Name:CytRx Corporation | |||||||||||||
| Full Title: A Multicenter, Randomized, Open-Label Phase 3 Study to Investigate the Efficacy and Safety of Aldoxorubicin Compared to Investigator’s Choice in Subjects with Metastatic, Locally Advanced, or Unres... | |||||||||||||
| Medical condition: Metastatic, Locally Advanced, or Unresectable Soft Tissue Sarcoma | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) ES (Prematurely Ended) FR (Prematurely Ended) IT (Prematurely Ended) NL (Prematurely Ended) PL (Prematurely Ended) DK (Prematurely Ended) BG (Prematurely Ended) GB (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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