- Trials with a EudraCT protocol (1,412)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1,412 result(s) found for: Cell body.
Displaying page 2 of 71.
EudraCT Number: 2013-000092-33 | Sponsor Protocol Number: PDTA02_24.05.2013 | Start Date*: 2013-10-23 | |||||||||||
Sponsor Name:Medizinische Universität Wien, Univ.Klinik.f.Dermatologie | |||||||||||||
Full Title: Enhanced efficacy of photodynamic therapy in combination with 5% imiquimod -a randomised, prospective, observer-blinded study in patients with non melanoma skin cancer | |||||||||||||
Medical condition: non melanoma skin cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-001634-26 | Sponsor Protocol Number: RPH001BEV01 | Start Date*: 2017-06-07 | |||||||||||
Sponsor Name:TRPHARM | |||||||||||||
Full Title: Phase I, Double Blind, Randomized, Parallel-Arm, Single-Dose, Pharmacokinetic and Safety Study of Bevacizumab-biosimilar (RPH-001) Compared to Bevacizumab-innovator (Avastin®, Roche) in Healthy Mal... | |||||||||||||
Medical condition: Non-Small Cell Lung Cancer | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005072-34 | Sponsor Protocol Number: VIT-2763-SCD-202 | Start Date*: 2021-07-26 | |||||||||||
Sponsor Name:Vifor (International) Inc. | |||||||||||||
Full Title: A Phase 2a, double-blind, randomised, placebo controlled, efficacy, and safety study of multiple doses of VIT-2763 in subjects with sickle cell disease (ViSion Serenity) | |||||||||||||
Medical condition: Sickle cell disease. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002572-41 | Sponsor Protocol Number: D9103C00001 | Start Date*: 2019-03-08 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Phase III, Randomized, Placebo-controlled, Double-blind, Multi-center, International Study of Durvalumab with Stereotactic Body Radiation Therapy (SBRT) for the Treatment of Patients with unresec... | |||||||||||||
Medical condition: Patients with unresected Stage I/II, lymph-node negative Non-small Cell Lung Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Trial now transitioned) GB (GB - no longer in EU/EEA) ES (Ongoing) FR (Trial now transitioned) DE (Trial now transitioned) NL (Trial now transitioned) BE (Trial now transitioned) IT (Trial now transitioned) GR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-016000-22 | Sponsor Protocol Number: XM22-04 | Start Date*: 2010-03-22 | ||||||||||||||||
Sponsor Name:BioGeneriX AG | ||||||||||||||||||
Full Title: Efficacy and safety of XM22 in patients with non small cell lung cancer receiving cisplatin / etoposide chemotherapy. A multinational, multicentre, randomised, double-blind placebo-controlled study | ||||||||||||||||||
Medical condition: Non Small Cell Lung Cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BG (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-000330-36 | Sponsor Protocol Number: TLK286.3020 | Start Date*: 2004-09-07 |
Sponsor Name:TELIK, INC. | ||
Full Title: Phase 3 Randomized Study of TLK286 versus Gefitinib (Iressa) as Third-Line Therapy in Locally Advanced or Metastatic Non-Small Cell Lung Cancer | ||
Medical condition: Treatment of patients with locally advanced or metastatic non-small cell lung cancer after failure of both platinum-based and docetaxel chemotherapies. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Ongoing) ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2021-005136-34 | Sponsor Protocol Number: THIO101 | Start Date*: 2022-11-16 | |||||||||||||||||||||
Sponsor Name:MAIA Biotechnology, Inc. | |||||||||||||||||||||||
Full Title: A Multicenter, Open-Label, Dose-Finding, Phase 2 Study Evaluating THIO Sequenced with Cemiplimab (LIBTAYO®) in Subjects with Advanced Non-Small Cell Lung Cancer (NSCLC) | |||||||||||||||||||||||
Medical condition: Non-Small Cell Lung Cancer | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: BG (Trial now transitioned) PL (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004114-35 | Sponsor Protocol Number: ETOP17-20 | Start Date*: 2022-02-21 | ||||||||||||||||
Sponsor Name:European Thoracic Oncology Platform (ETOP) | ||||||||||||||||||
Full Title: A multicentre single-arm phase II trial assessing the safety and efficacy of first-line osimertinib and locally ablative radiotherapy in patients with synchronous oligo-metastatic EGFR-mutant non-s... | ||||||||||||||||||
Medical condition: Treatment naïve patients with synchronous, oligo-metastatic (primary tumour and maximum 5 metastases) EGFR-mutant (exon 19 deletion or exon 21 L858R) NSCLC with or without T790M resistance mutation | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) IT (Prematurely Ended) NL (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001792-39 | Sponsor Protocol Number: G300505 | Start Date*: 2012-01-04 | |||||||||||||||||||||
Sponsor Name:GTx, Inc. | |||||||||||||||||||||||
Full Title: Phase III, Randomized, Double-Blind, Placebo-Controlled Study of the Effect of GTx-024 on Muscle Wasting in Patients with Non-Small Cell Lung Cancer on First Line Platinum Plus a Non-Taxane Chemoth... | |||||||||||||||||||||||
Medical condition: Cachexia, muscle wasting in patients with Non-Small Cell Lung Cancer | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: PL (Completed) HU (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002552-24 | Sponsor Protocol Number: PKAPIR | Start Date*: 2016-12-16 | |||||||||||
Sponsor Name:Centre Georges François Leclerc | |||||||||||||
Full Title: Pemetrexed (Alimta®) in maintenance in patients with impaired renal function: multicenter randomized Phase 4 study comparing two strategies for dose calculation | |||||||||||||
Medical condition: Patients with non-small lung cell cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001559-30 | Sponsor Protocol Number: SMKV-013-CP4 | Start Date*: 2017-09-13 | |||||||||||
Sponsor Name:Fresenius Kabi Deutschland GmbH | |||||||||||||
Full Title: Efficacy of long-term parenteral nutrition with SmofKabiven® E concomitant to chemo- and/or immunotherapy: A prospective, randomised, controlled, open, multicentre, two-stage, adaptive clinical tri... | |||||||||||||
Medical condition: Metastatic Non-Small Cell Lung Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002359-27 | Sponsor Protocol Number: D5161C00003 | Start Date*: 2017-11-13 | |||||||||||||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||||||||||||
Full Title: A Multicentre, Open-label, Single-arm, Molecular Profiling Study of Patients with EGFR Mutation-positive Locally Advanced or Metastatic NSCLC Treated with Osimertinib | |||||||||||||||||||||||
Medical condition: EGFR mutation-positive locally advanced or metastatic non-small cell lung cancer not amenable to curative surgery or radiotherapy | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: ES (Ongoing) IT (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-003011-22 | Sponsor Protocol Number: ETOP_14-18 | Start Date*: 2019-10-10 | |||||||||||
Sponsor Name:ETOP (European Thoracic Oncology Platform) | |||||||||||||
Full Title: A multicentre single arm phase II trial assessing the efficacy of immunotherapy, chemotherapy and stereotactic radiotherapy to metastases followed by definitive surgery or radiotherapy to the prima... | |||||||||||||
Medical condition: Synchronous oligo-metastatic Non-Small Cell Lung Cancer (NSCLC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) NL (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002545-38 | Sponsor Protocol Number: 68943 | Start Date*: 2019-09-13 | |||||||||||||||||||||
Sponsor Name:Bispebjerg Hospital, Department of Dermatology | |||||||||||||||||||||||
Full Title: Biodistribution of ablative fractional laser-assisted topical delivery of Vismodegib in basal cell carcinomas. | |||||||||||||||||||||||
Medical condition: Basal cell carcinoma Simple nodular basal cell carcinoma at any body locations | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-004783-30 | Sponsor Protocol Number: ARD12858-MOZ23510 | Start Date*: 2013-01-21 | |||||||||||
Sponsor Name:Sanofi aventis recherche et développement | |||||||||||||
Full Title: A pilot, exploratory, randomized, phase 2 safety study evaluating tumor cell (plasma cell) mobilization and apheresis product contamination in plerixafor plus non-pegylated G-CSF mobilized patients... | |||||||||||||
Medical condition: Multiple Myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) LT (Completed) SE (Completed) EE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-001903-42 | Sponsor Protocol Number: IPH5201-201 | Start Date*: 2023-03-07 | |||||||||||||||||||||
Sponsor Name:Innate Pharma SA | |||||||||||||||||||||||
Full Title: A Phase II Multicenter, open label, non-randomized study of neoadjuvant and Adjuvant Treatment with IPH5201 and durvalumab in patients with resectable, early-Stage (II to IIIA) Non-Small Cell Lung ... | |||||||||||||||||||||||
Medical condition: Non-Small Cell Lung Cancer | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FR (Trial now transitioned) HU (Trial now transitioned) PL (Trial now transitioned) GR (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000662-65 | Sponsor Protocol Number: D5164C00001 | Start Date*: 2015-08-12 | |||||||||||||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||||||||||||
Full Title: A Phase III, double-blind, randomized, placebo-controlled multi-centre, study to assess the efficacy and safety of AZD9291 versus Placebo, in patients with Epidermal Growth Factor Receptor Mutation... | |||||||||||||||||||||||
Medical condition: Stage IB-IIIA non-small cell lung carcinoma, with a centrally confirmed, common sensitising EGFR mutations (Ex19del and L858R either alone or in combination with other EGFR mutations), following co... | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: BE (Trial now transitioned) IT (Completed) DE (Trial now transitioned) HU (Completed) NL (Ongoing) FR (Trial now transitioned) ES (Ongoing) PL (Trial now transitioned) SE (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003953-13 | Sponsor Protocol Number: PPHM1202 | Start Date*: 2014-04-01 | ||||||||||||||||
Sponsor Name:Peregrine Pharmaceuticals, Inc. | ||||||||||||||||||
Full Title: A Phase III, Randomized, Double-Blind, Placebo-Controlled Multicenter Trial of Bavituximab Plus Docetaxel versus Docetaxel Alone in Patients with Previously Treated Stage IIIb/IV Non-Squamous Non... | ||||||||||||||||||
Medical condition: Stage IIIb/IV Non-Squamous Non Small-Cell Lung Cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) IT (Prematurely Ended) BE (Prematurely Ended) HU (Prematurely Ended) ES (Completed) GR (Prematurely Ended) RO (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-005096-85 | Sponsor Protocol Number: XM22-ONC-40041 | Start Date*: 2015-05-25 | ||||||||||||||||
Sponsor Name:Merckle GmbH | ||||||||||||||||||
Full Title: Safety and Efficacy of LONQUEX® (Lipegfilgrastim) in Comparison to Pegfilgrastim (Neulasta®, Amgen Inc.) and Placebo in Patients with Non-Small-Cell Lung Cancer Receiving First-Line Chemotherapy | ||||||||||||||||||
Medical condition: Advanced squamous or non-squamous non-small-cell lung cancer (NSCLC) Stage IIIB/IV | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SK (Completed) HU (Completed) LV (Completed) PL (Prematurely Ended) GR (Completed) BG (Completed) ES (Completed) HR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-002029-12 | Sponsor Protocol Number: ETOP10-16 | Start Date*: 2017-04-24 | |||||||||||||||||||||
Sponsor Name:ETOP IBCSG Partners Foundation | |||||||||||||||||||||||
Full Title: A randomised phase II trial of osimertinib and bevacizumab versus osimertinib alone as second-line treatment in stage IIIb-IVb NSCLC with confirmed EGFRm and T790M | |||||||||||||||||||||||
Medical condition: Patients with locally advanced or metastatic (stage IIIb-IVb) EGFRm (exon 19 deletion or exon 21 L858R) NSCLC with T790M resistance mutation at progression on prior EGFR TKI therapy | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IE (Completed) ES (Ongoing) NL (Completed) | |||||||||||||||||||||||
Trial results: View results |
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