- Trials with a EudraCT protocol (775)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
775 result(s) found for: Cancer survival rates.
Displaying page 1 of 39.
| 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: 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: 2018-002717-35 | Sponsor Protocol Number: P170920J | Start Date*: 2018-12-13 | |||||||||||
| Sponsor Name:ASSISTANCE PUBLIQUE - HÔPITAUX DE PARIS (AP-HP) | |||||||||||||
| Full Title: Non inferiority multicenter phase III randomized trial comparing preoperative chemotherapy only to chemoradiotherapy for locally advanced resectable rectal cancer (intergroup FRENCH-GRECCAR- PRODIGE) | |||||||||||||
| Medical condition: Adults ≥ 18 years with middle or low locally advanced resectable rectal carcinoma | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| 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: 2016-005187-34 | Sponsor Protocol Number: CCR4644 | Start Date*: 2017-09-11 |
| Sponsor Name:The Royal Marsden NHS Foundation Trust | ||
| Full Title: Stereotactic body radiotherapy with immunotherapy in early stage non-small cell lung cancer: tolerability and lung effects | ||
| Medical condition: Non small-cell lung cancer (NSCLC) Stage: T1-3( ≤5cm)N0M0) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-001419-25 | Sponsor Protocol Number: GastricCHIMERAtrial | Start Date*: 2021-04-09 | |||||||||||
| Sponsor Name:Jagiellonian University Medical College | |||||||||||||
| Full Title: Preoperative intraperitoneal chemotherapy in adjuvant hyperthermia adjunctive therapy in advanced gastric cancer with high-risk of peritoneal recurrence - a multicentre randomized trial | |||||||||||||
| Medical condition: Gastric Carcinoma | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-021434-55 | Sponsor Protocol Number: FE 200486 CS35A | Start Date*: 2010-11-11 | |||||||||||
| Sponsor Name:Ferring Pharmaceuticals A/S | |||||||||||||
| Full Title: An Open-label, Multi-Centre, Extension Trial, Evaluating the Long-Term Progression-Free Survival of Degarelix or Goserelin Three-Month Dosing Regimens in Patients with Prostate Cancer Requiring And... | |||||||||||||
| Medical condition: Prostate cancer | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: HU (Prematurely Ended) GB (Prematurely Ended) FI (Prematurely Ended) NL (Prematurely Ended) CZ (Completed) BE (Completed) DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-005142-29 | Sponsor Protocol Number: UC-0107/1718 | Start Date*: 2018-08-30 |
| Sponsor Name:UNICANCER | ||
| Full Title: PD-(L)1 iNhibitors with concurrent IRadiation at VAried tumour sites in advanced Non-small cell lung cAncer | ||
| Medical condition: Advanced (stage IIIB/IIIC/IV) NSCLC patients eligible for treatment with a PD-1 or PD-L1 antagonist according to the European Marketing Authorisation in a first line or a second line | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-005210-18 | Sponsor Protocol Number: EFFIPEC01 | Start Date*: 2021-03-28 | |||||||||||
| Sponsor Name:Uppsala University | |||||||||||||
| Full Title: EFFIPEC – Efficacy of Hyperthermic Intraperitoneal Chemotherapy Single-arm Phase I study, followed by an open-label, randomized, controlled registry-based Phase III trial | |||||||||||||
| Medical condition: Colorectal cancer | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-004819-31 | Sponsor Protocol Number: IN-CRC-001 | Start Date*: 2021-05-19 | |||||||||||
| Sponsor Name:IN3BIO | |||||||||||||
| Full Title: A Phase I/II, multi-centre, open-label, adaptive design, umbrella study assessing the safety, tolerability, immunogenicity and efficacy of IN01 in combination with small-molecule inhibitors in two ... | |||||||||||||
| Medical condition: colorectal cancer at a metastatic stage, eligible for a second line treatment and presenting with a constitutive BRAF or RAS mutation | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BG (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-003301-97 | Sponsor Protocol Number: GO41767 | Start Date*: 2020-04-15 | ||||||||||||||||
| Sponsor Name:F. Hoffmann-La Roche Ltd | ||||||||||||||||||
| Full Title: A PHASE III, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY OF ATEZOLIZUMAB PLUS CARBOPLATIN AND ETOPOSIDE WITH OR WITHOUT TIRAGOLUMAB (ANTI-TIGIT ANTIBODY) IN PATIENTS WITH UNTREATED EXTENSIVE... | ||||||||||||||||||
| Medical condition: Small cell lung cancer (SCLC) | ||||||||||||||||||
|
||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) GB (GB - no longer in EU/EEA) PL (Trial now transitioned) AT (Completed) HU (Completed) BE (Completed) ES (Ongoing) GR (Trial now transitioned) IT (Trial now transitioned) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2019-002971-32 | Sponsor Protocol Number: PROICM2019-11PRA | Start Date*: 2020-07-27 |
| Sponsor Name:Institut Regional du Cancer de Montpellier | ||
| Full Title: A Double blind randomized phase III study of pravastatin vs placebo as primary prevention of severe subcutaneous breast fibrosis in hyper-radiosensitive identified patients with breast cancer | ||
| Medical condition: Radio-induced fibrosis in breast cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: FR (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-003819-56 | Sponsor Protocol Number: 26193789 | Start Date*: 2020-06-12 | |||||||||||||||||||||
| Sponsor Name:Centre for Surgical Science | |||||||||||||||||||||||
| Full Title: Effects of intravenous administered iron in non-anemic iron deficient patients with colorectal cancer. A double blinded clinical randomized trial. | |||||||||||||||||||||||
| Medical condition: Iron-deficiency in colorectal cancer | |||||||||||||||||||||||
|
|||||||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DK (Trial now transitioned) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2016-000857-11 | Sponsor Protocol Number: 345-449 | Start Date*: 2016-05-27 |
| Sponsor Name:Bank of Cyprus Oncology Centre | ||
| Full Title: A Phase II study of Switch Maintenance Pembrolizumab in patients with Non Small Cell Lung Cancer (NSCLC) who do not progress after First Line Platinum Doublet Chemotherapy | ||
| Medical condition: Non small cell lung cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: CY (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-004433-26 | Sponsor Protocol Number: 3638 | Start Date*: 2016-05-04 | |||||||||||||||||||||
| Sponsor Name:North Bristol NHS Trust | |||||||||||||||||||||||
| Full Title: Zoledronic acid in the management of malignant pleural mesothelioma - a feasibility study | |||||||||||||||||||||||
| Medical condition: Malignant pleural mesothelioma | |||||||||||||||||||||||
|
|||||||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2006-000366-36 | Sponsor Protocol Number: TLK286.3025 | Start Date*: 2006-06-07 | |||||||||||
| Sponsor Name:Telik, Inc. | |||||||||||||
| Full Title: Phase 3 randomized study of TLK286 (Telcyta™) in combination with liposomal doxorubicin (Doxil®/Caelyx®) versus liposomal doxorubicin (Doxil®/Caelyx®) as second-line therapy in platinum refractory ... | |||||||||||||
| Medical condition: platinum refractory or resistant ovarian cancer | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: GB (Completed) BE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| 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 | |||||||||||||
| 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: 2007-004102-27 | Sponsor Protocol Number: SCI-RP-Pan-P2-001 | Start Date*: 2008-02-20 | ||||||||||||||||
| Sponsor Name:SciClone Pharmaceuticals, Inc. | ||||||||||||||||||
| Full Title: A Randomized, Double Blind, Placebo Controlled, Phase II Study Evaluating the Efficacy and Safety of RP101 in Combination with Gemcitabine Administered as First-Line Treatment to Subjects with Unre... | ||||||||||||||||||
| Medical condition: metastatic pancreatic cancer | ||||||||||||||||||
|
||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: HU (Prematurely Ended) ES (Ongoing) NL (Prematurely Ended) DE (Prematurely Ended) GB (Prematurely Ended) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2015-005556-10 | Sponsor Protocol Number: CA209-577 | Start Date*: 2016-05-24 | ||||||||||||||||||||||||||||||||||||
| Sponsor Name:Bristol-Myers Squibb International Corporation | ||||||||||||||||||||||||||||||||||||||
| Full Title: A Randomized, Multicenter, Double Blind, Phase III Study of Adjuvant Nivolumab or Placebo in Subjects with Resected Esophageal, or Gastroesophageal Junction Cancer | ||||||||||||||||||||||||||||||||||||||
| Medical condition: Subjects with resected adenocarcinoma or squamous cell carcinoma esophageal or gastroesophageal junction cancer | ||||||||||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
| Trial protocol: HU (Completed) ES (Ongoing) CZ (Trial now transitioned) GB (GB - no longer in EU/EEA) IE (Trial now transitioned) DE (Trial now transitioned) BE (Trial now transitioned) DK (Trial now transitioned) NL (Trial now transitioned) RO (Trial now transitioned) FR (Trial now transitioned) IT (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||||||||||||
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.