- Trials with a EudraCT protocol (7,132)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
7,132 result(s) found for: Cancer survival.
Displaying page 1 of 357.
| EudraCT Number: 2012-001224-35 | Sponsor Protocol Number: TaxOvar | Start Date*: 2012-08-13 | |||||||||||
| Sponsor Name:Vejle Hospital | |||||||||||||
| Full Title: Cabazitaxel in platinum refractory ovarian cancer. A phase II trial | |||||||||||||
| Medical condition: Platinum refractory ovarian cancer | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: DK (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-003072-12 | Sponsor Protocol Number: 01082018 | Start Date*: 2019-02-05 | |||||||||||||||||||||||||||||||
| Sponsor Name:rigshospitalet | |||||||||||||||||||||||||||||||||
| Full Title: Radiation Therapy Planning by Multi-parametric PET/MRI Imaging in patients with cervical cancer | |||||||||||||||||||||||||||||||||
| Medical condition: cervical cancer | |||||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2018-003691-12 | Sponsor Protocol Number: TUD-CIRC01-071 | Start Date*: 2019-12-04 | ||||||||||||||||
| Sponsor Name:Technische Universität Dresden | ||||||||||||||||||
| Full Title: Circulating tumour DNA based decision for adjuvant treatment in colon cancer stage II evaluation (CIRCULATE) AIO-KRK-0217 | ||||||||||||||||||
| Medical condition: Colon cancer stage II | ||||||||||||||||||
|
||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2005-003327-39 | Sponsor Protocol Number: KKSH-14 | Start Date*: 2006-04-21 |
| Sponsor Name:Martin-Luther-University | ||
| Full Title: Integration of 3D-conformal, local radiotherapy (3DCRT) to metastatic sites in a paclitaxel weekly chemotherapy regimen in oligometastatic breast cancer patients: a phase I- and randomised phase II... | ||
| Medical condition: oligometastatic breast cancer | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: DE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-000193-38 | Sponsor Protocol Number: ENGOT-EN1/FANDANGO | Start Date*: 2016-06-20 | ||||||||||||||||||||||||||||||||||||
| Sponsor Name:Nordic Society of Gynaecological Oncology (NSGO) - CTU | ||||||||||||||||||||||||||||||||||||||
| Full Title: ENGOT-EN1/FANDANGO: A randomized phase II trial of first-line combination chemotherapy with nintedanib / placebo for patients with advanced or recurrent endometrial cancer. | ||||||||||||||||||||||||||||||||||||||
| Medical condition: Histological confirmed endometrial cancer. (FIGO 2009) stage 3C2 or stage 4 or relapsed after adjuvant therapy for stage 1-3 disease. | ||||||||||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||||||||||||
| Trial protocol: SE (Completed) DK (Prematurely Ended) DE (Completed) FI (Completed) BE (Completed) FR (Completed) | ||||||||||||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2014-002014-22 | Sponsor Protocol Number: ONK-MAP/AZD2281-01 | Start Date*: 2014-05-27 | |||||||||||
| Sponsor Name:Országos Onkológiai Intézet | |||||||||||||
| Full Title: An open label, single center, non-randomised, phase II study of efficacy Olaparib in patients with BRCA mutation posistive previously treated advanced ocarium cancer | |||||||||||||
| Medical condition: advanced ovarian cancer | |||||||||||||
|
|||||||||||||
| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: HU (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-001748-23 | Sponsor Protocol Number: SGM-LARRC | Start Date*: 2019-08-07 | ||||||||||||||||
| Sponsor Name:Leiden University Medical Center | ||||||||||||||||||
| Full Title: Multicenter, open-label, controlled, parallel arms clinical study on the performance of SGM-101, a fluorochrome-labeled anti-carcino-embryonic antigen (CEA) monoclonal antibody, for locally advance... | ||||||||||||||||||
| Medical condition: Locally advanced rectal cancer Recurrent rectal cancer | ||||||||||||||||||
|
||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2011-000299-33 | Sponsor Protocol Number: AGO-GYN8 | Start Date*: Information not available in EudraCT | ||||||||||||||||
| Sponsor Name:AGO Research GmbH | ||||||||||||||||||
| Full Title: Efficacy, tolerability and safety of Temsirolimus in women with platinum-refractory ovarian carcinoma or advanced endometrial carcinoma | ||||||||||||||||||
| Medical condition: platinum-refractory ovarian carcinoma or advanced endometrial carcinoma | ||||||||||||||||||
|
||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: DE (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2021-003542-21 | Sponsor Protocol Number: ALADDIN | Start Date*: 2022-02-28 |
| Sponsor Name:ARTIC - Association pour la Recherche de Thérapeutiques Innovantes en Cancérologie | ||
| Full Title: Evaluation of dAroLutamide Addition to anDrogen Deprivation therapy and radIatioN therapy in newly diagnosed prostate cancer with pelvic lymph nodes metastases | ||
| Medical condition: Prostate cancer with pelvic lymph nodes metastases. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-001661-32 | Sponsor Protocol Number: VeTo | Start Date*: 2012-07-05 | |||||||||||||||||||||
| Sponsor Name:Vejle Hospital, Dept. of Oncology | |||||||||||||||||||||||
| Full Title: Veliparib (ABT888) and Topotecan (Hycamtin®) for Patients with Platinum-Resistant or Partially Platinum-Sensitive Relapse of Epithelial Ovarian Cancer with Negative or Unknown BRCA Status | |||||||||||||||||||||||
| Medical condition: Relapsed epithelial, platinum resistant ovarian cancer with negative or unknown BRCA status | |||||||||||||||||||||||
|
|||||||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2010-023613-61 | Sponsor Protocol Number: IPR/24 | Start Date*: 2011-06-13 | |||||||||||
| Sponsor Name:MOLMED | |||||||||||||
| Full Title: NGR018: Randomized phase II study of NGR-hTNF plus pegylated liposomal doxorubicin (PLD) versus PLD in platinum-resistant ovarian cancer | |||||||||||||
| Medical condition: Advanced or metastatic platinum-resistant ovarian cancer patients | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: IT (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-022482-95 | Sponsor Protocol Number: BGOG-ov-5 | Start Date*: 2012-02-07 | |||||||||||||||||||||
| Sponsor Name:Belgian Gynaecological Oncolgy Group | |||||||||||||||||||||||
| Full Title: BGOG-OV5:Phase II study of weekly Paclitaxel/Carboplatin in combination with prophylactic G-CSF in the treatment of gynaecological cancers. | |||||||||||||||||||||||
| Medical condition: recurrence of ovarian, fallopian tube or peritoneal carcinoma, cervical carcinoma or endometrial carcinoma | |||||||||||||||||||||||
|
|||||||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2019-001077-87 | Sponsor Protocol Number: IJB-RT-HNC-001 | Start Date*: 2019-08-08 | |||||||||||
| Sponsor Name:Institut Jules Bordet | |||||||||||||
| Full Title: Patient reported outcomes in term of swallowing and quality of life after prophylactic versus reactive percutaneous endoscopic gastrostomy tube placement in advanced head and neck cancer patients t... | |||||||||||||
| Medical condition: advanced head and neck cancer | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-005091-36 | Sponsor Protocol Number: 2020-005091-36 | Start Date*: 2021-08-30 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:Stichting Catharina Hospital | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: Signal TrAnsduction Pathway activity analysis for OVarian cancER treatment. STAPOVER study | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Ovarian cancer | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Population Age: Elderly | Gender: Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: NL (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2021-000398-10 | Sponsor Protocol Number: EFC16133 | Start Date*: 2022-04-19 | |||||||||||
| Sponsor Name:Sanofi-aventis recherche & développement | |||||||||||||
| Full Title: A randomized, multicenter, double-blind, Phase 3 study of amcenestrant (SAR439859) versus tamoxifen for the treatment of patients with hormone receptor-positive, human epidermal growth factor 2-neg... | |||||||||||||
| Medical condition: Breast cancer | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) HU (Prematurely Ended) EE (Prematurely Ended) BE (Prematurely Ended) PT (Prematurely Ended) DK (Prematurely Ended) IT (Prematurely Ended) ES (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-004686-32 | Sponsor Protocol Number: v2.0 | Start Date*: 2014-08-05 | |||||||||||||||||||||
| Sponsor Name:Leiden University Medical Center | |||||||||||||||||||||||
| Full Title: A Phase III double-blind placebo-controlled Randomised Trial of Aspirin on Recurrence and Survival in Colon Cancer Patients | |||||||||||||||||||||||
| Medical condition: Patients must have TNM stage that is one of the following: pT3-4; N0-2 and M0, or pT1-2 and N1-2 (UICC stage II and III) (in case of >1 tumour: largest tumour is stage II or III) | |||||||||||||||||||||||
|
|||||||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: NL (Trial now transitioned) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2011-003078-10 | Sponsor Protocol Number: SPCG 16 | Start Date*: 2011-11-02 | |||||||||||
| Sponsor Name:SPCG | |||||||||||||
| Full Title: SPCG 16 Sensi-cab Randomized phase III trial comparing cabazitaxel in combination with hormone therapy to hormone therapy alone in metastatic prostate cancer | |||||||||||||
| Medical condition: Patients diagnosed with metastatic or high risk(PSA>100 or N1) prostate cancer. | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: SE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-006831-10 | Sponsor Protocol Number: 1199.15 | Start Date*: Information not available in EudraCT | ||||||||||||||||||||||||||
| Sponsor Name:Boehringer Ingelheim Pharma GmbH & Co. KG | ||||||||||||||||||||||||||||
| Full Title: Multicenter, randomised, double-blind Phase III trial to investigate the efficacy and safety of BIBF 1120 in combination with carboplatin and paclitaxel compared to placebo plus carboplatin and pac... | ||||||||||||||||||||||||||||
| Medical condition: Advanced ovarian cancer, fallopian tube cancer or primary peritoneal cancer | ||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||
| Trial protocol: DE (Completed) FR (Completed) SE (Completed) BE (Completed) PT (Completed) SK (Completed) DK (Completed) AT (Completed) NL (Completed) FI (Completed) PL (Completed) IT (Completed) GR (Completed) CZ (Completed) ES (Completed) GB (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2012-005546-38 | Sponsor Protocol Number: AEZS-108-050 | Start Date*: 2013-10-14 | ||||||||||||||||
| Sponsor Name:Aeterna Zentaris GmbH | ||||||||||||||||||
| Full Title: Randomised controlled study comparing AEZS-108 with doxorubicin as second line therapy for locally advanced, recurrent or metastatic endometrial cancer | ||||||||||||||||||
| Medical condition: Endometrial cancer, advanced, recurrent or metastatic | ||||||||||||||||||
|
||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: CZ (Completed) BE (Completed) GB (Completed) AT (Completed) DE (Completed) ES (Completed) IE (Completed) IT (Completed) BG (Completed) NL (Completed) PL (Completed) DK (Completed) FI (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2010-022902-41 | Sponsor Protocol Number: BIG4-11/BO25126/TOC4939g | Start Date*: 2011-09-26 | |||||||||||
| Sponsor Name:F. Hoffmann-La Roche Ltd. | |||||||||||||
| Full Title: A randomized multicenter, double-blind, placebo-controlled comparison of chemotherapy plus trastuzumab plus placebo versus chemotherapy plus trastuzumab plus pertuzumab as adjuvant therapy in pa... | |||||||||||||
| Medical condition: Patients with operable HER2-positive primary breast cancer | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) HU (Completed) CZ (Completed) ES (Ongoing) FR (Completed) IE (Completed) SE (Completed) DK (Completed) SI (Completed) NL (Completed) BE (Completed) SK (Completed) AT (Completed) IT (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
| Download Options: | |
|---|---|
| Number of Trials to download: | |
| Download Content: | |
| Download Format: | |
| Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. | |
Query did not match any studies.