- Trials with a EudraCT protocol (6)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
6 result(s) found for: Miscellaneous and site unspecified neoplasms benign.
Displaying page 1 of 1.
| EudraCT Number: 2011-005718-12 | Sponsor Protocol Number: AP26113-11-101 | Start Date*: 2012-07-12 | |||||||||||||||||||||||||||||||
| Sponsor Name:ARIAD Pharmaceuticals, Inc. | |||||||||||||||||||||||||||||||||
| Full Title: A Phase 1/2 Study of the Safety, Tolerability, Pharmacokinetics and Preliminary Anti-Tumor Activity of the Oral ALK/EGFR Inhibitor AP26113 | |||||||||||||||||||||||||||||||||
| Medical condition: Dose Escalation Phase: Histologically confirmed advanced malignancies. All histologies except leukaemia. Dose Expansion Phase: Non-small cell lung cancer (NSCLC) | |||||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2020-000854-85 | Sponsor Protocol Number: CA045-020 | Start Date*: 2021-04-19 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:Bristol-Myers Squibb International Corporation | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: Phase 1/2 Study of Bempegaldesleukin in Combination with Nivolumab in Children, Adolescents, and Young Adults with Recurrent or Refractory Malignancies (PIVOT IO 020) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Recurrent or Refractory pediatric cancer | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: FR (Prematurely Ended) ES (Prematurely Ended) DE (Completed) IT (Prematurely Ended) Outside EU/EEA | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2015-004727-31 | Sponsor Protocol Number: IRST100.26 | Start Date*: 2016-03-16 | |||||||||||
| Sponsor Name:ISTITUTO SCIENTIFICO ROMAGNOLO PER LO STUDIO E LA CURA DEI TUMORI (IRST) S.R.L. IRCCS | |||||||||||||
| Full Title: RANDOMIZED PHASE II TRIAL IN SSTr2 POSITIVE TUMORS TO OPTIMIZE THE INTERVAL BETWEEN CYCLES OF PRRT WITH 177LU DOTATATE (LUTHREE) | |||||||||||||
| Medical condition: SSTr2 POSITIVE TUMORS | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-006538-16 | Sponsor Protocol Number: A6181114 | Start Date*: 2007-03-30 | |||||||||||
| Sponsor Name:Pfizer Inc, 235 East 42nd Street, New York, NY 10017, US | |||||||||||||
| Full Title: AN OPEN-LABEL SUNITINIB MALATE (SU011248) CONTINUATION PROTOCOL FOR PATIENTS WHO HAVE COMPLETED A PRIOR SUNITINIB STUDY AND ARE JUDGED BY THE INVESTIGATOR TO HAVE THE POTENTIAL TO BENEFIT FROM SUNI... | |||||||||||||
| Medical condition: Malignant Gastrointestinal Stromal Tumor (GIST), Metastatic Breast Cancer, Metastatic Renal Cell Cancer, Pancreatic Neuroendocrine Tumor, Hepatocellular Carcinoma, Prostate Cancer, Thyroid Cancer, ... | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) BE (Completed) FR (Completed) DK (Prematurely Ended) GB (Completed) NL (Prematurely Ended) BG (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2004-001093-11 | Sponsor Protocol Number: A6181030 | Start Date*: 2004-12-24 | |||||||||||
| Sponsor Name:Pfizer Global Research and Development | |||||||||||||
| Full Title: A Treatment Protocol for Patients Continuing from a Prior SU011248 Protocol | |||||||||||||
| Medical condition: This is an open-label treatment protocol for patients who have participated in other SU011248 protocols to completion and are believed to have the potential to derive clinical benefit from SU011248... | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) ES (Prematurely Ended) NL (Completed) SE (Completed) GR (Prematurely Ended) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-002604-17 | Sponsor Protocol Number: BAY 43-9006 / 12311 | Start Date*: 2009-12-14 | |||||||||||
| Sponsor Name:Bayer HealthCare AG, D-51368 Leverkusen, Germany | |||||||||||||
| Full Title: Sorafenib Long Term Extension Program (STEP) | |||||||||||||
| Medical condition: Various cancer indications/types (e.g. Renal Cell Carcinoma, Hepatoma Carcinoma, Melanoma and other cancer types). Patients who remain actively treated in a Bayer/Onyx sponsored Clinical Trial tha... | |||||||||||||
|
|||||||||||||
| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) DE (Completed) ES (Completed) IT (Completed) PL (Completed) GB (Completed) BE (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.