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Miss Angela Casbard
Hafan
Prosiectau
Setiau Data Ymchwil
Miss
Angela
Casbard
Prosiectau fel Prif Ymchwiliwr
1 o 2
A randomised double blind placebo controlled phase II study of fulvestrant with or without the addition of vandetanib as treatment for patients with metastatic breast cancer resistant to aromatase inhibitor therapy - FURVA CRUK
-
Cyllidwr:
Cancer Research UK
(
01.10.2014
-
30.09.2017
)
A randomised phase II trial of oral vinorelbine as second-line therapy for patients with malignant pleural mesothelioma - VIM
-
Cyllidwr:
Cancer Research UK
,
-
Cyllidwr:
University of Leicester
(
01.11.2013
-
31.12.2020
)
A phase 1b/randomised placebo controlled phase II trial of fulvestrant +/- AZD5363 in postmenopausal women with advanced breast cancer previously treated with a third generation aromatase inhibitor - FAKTION CRUK
-
Cyllidwr:
Cancer Research UK
(
01.10.2013
-
31.10.2019
)
A randomised double blind placebo controlled phase II study of fulvestrant with or without the addition of vandetanib as treatment for patients with metastatic breast cancer resistant to aromatase inhibitor therapy - FURVA AZ
-
Cyllidwr:
AstraZeneca UK Ltd
(
01.10.2014
-
30.09.2020
)
Phase II evaluation of cediranib in combination with paclitaxel of olaparib in advanced/metastatic endometrial carcinoma (COPELIA)
-
Cyllidwr:
AstraZeneca UK Ltd
(
01.10.2017
-
30.06.2022
)
Prosiectau fel Cyd-Ymchwiliwr
1 o 2
A randomised phase II trial of carboplation and gemcitabane +/- vandetanib in first line treatment of advanced urothelial cell cancer in patients who are not suitable to receive cisplatin - TOUCAN
-
Cyllidwr:
AstraZeneca UK Ltd
,
-
Cyllidwr:
AstraZeneca UK Ltd
(
19.10.2009
-
30.09.2020
)
TOTEM: A phase I/II single-arm trial to evaluate the combination of cisplatin and gemcitabine with the mTOR inhibitor temsirolimus for first-line treatment of patients with advanced transitional cell carcinoma of the urothelium
-
Cyllidwr:
Pfizer Ltd
(
07.11.2011
-
30.09.2019
)
SKOPOS
-
Cyllidwr:
Velindre NHS Trust
(
01.01.2013
-
31.12.2016
)
A feasibility study to inform the design of a randomised controlled trial to identify the most clinically and cost effective length of anticoagulation with low molecular weight heparin in the treatment of Cancer Associated Thrombosis (ALICAT)
-
Cyllidwr:
National Institute for Health Research
(
01.03.2013
-
28.02.2015
)
Folfera Trial
-
Cyllidwr:
AstraZeneca UK Ltd
,
-
Cyllidwr:
AstraZeneca UK Ltd
(
01.09.2009
-
30.09.2020
)
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Diweddarwyd y tro diwethaf ar 2021-11-01 am 22:06