SEITZ, Christian, Žana BUMBULIENE, Ana Rosa COSTA, Oskari HEIKINHEIMO, Andrea HEWEKER, Robert HUDEČEK, Yves JACQUEMYN, Gian Benedetto MELIS, Pooja PARASHAR, Tomasz RECHBERGER, Antonio Cano SÁNCHEZ, Bart van AKENL, János ZATIK a Kristina GEMZELL-DANIELSSON. Rationale and design of ASTEROID 2, a randomized, placebo- and active comparator-controlled study to assess the efficacy and safety of vilaprisan in patients with uterine fibroids. CONTEMPORARY CLINICAL TRIALS. New York: Elsevier Science, 2017, roč. 55, APR 2017, s. 56-62. ISSN 1551-7144. Dostupné z: https://dx.doi.org/10.1016/j.cct.2017.02.002.
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Základní údaje
Originální název Rationale and design of ASTEROID 2, a randomized, placebo- and active comparator-controlled study to assess the efficacy and safety of vilaprisan in patients with uterine fibroids
Autoři SEITZ, Christian (276 Německo), Žana BUMBULIENE (440 Litva), Ana Rosa COSTA (620 Portugalsko), Oskari HEIKINHEIMO (246 Finsko), Andrea HEWEKER (276 Německo), Robert HUDEČEK (203 Česká republika, garant, domácí), Yves JACQUEMYN (56 Belgie), Gian Benedetto MELIS (380 Itálie), Pooja PARASHAR (578 Norsko), Tomasz RECHBERGER (616 Polsko), Antonio Cano SÁNCHEZ (724 Španělsko), Bart van AKENL (528 Nizozemské království), János ZATIK (348 Maďarsko) a Kristina GEMZELL-DANIELSSON (752 Švédsko).
Vydání CONTEMPORARY CLINICAL TRIALS, New York, Elsevier Science, 2017, 1551-7144.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor 30104 Pharmacology and pharmacy
Stát vydavatele Nizozemské království
Utajení není předmětem státního či obchodního tajemství
Impakt faktor Impact factor: 2.658
Kód RIV RIV/00216224:14110/17:00097318
Organizační jednotka Lékařská fakulta
Doi http://dx.doi.org/10.1016/j.cct.2017.02.002
UT WoS 000397692100008
Klíčová slova anglicky Vilaprisan; Progesterone receptor modulator;Uterine fibroids;Ulipristal acetate;Amenorrhoea
Štítky EL OK
Příznaky Mezinárodní význam, Recenzováno
Změnil Změnila: Soňa Böhmová, učo 232884. Změněno: 17. 5. 2018 16:28.
Anotace
Background: Uterine fibroids (UFs) may be treated with progesterone receptor modulators (PRMs), which have been shown to reduce heavy menstrual bleeding and the size of UFs. To date, one PRM (ulipristal acetate) has received regulatory approval for the treatment of UFs; therapy comprises intermittent treatment courses of up to 3 months each, followed by a break to allowtwo menstruations to occur.Wereport the design of ASTEROID (Assess Safety and efficacy of vilaprisan in patients with uTERine fibrOIDs) 2, a phase 2 study examining the efficacy and safety of a novel PRM, vilaprisan, in women with UFs. Methods/design: In this randomized multi-arm study, vilaprisan (2 mg daily) will be administered in different regimens: continuous treatment for 12 or 24 weeks, or two 12-week treatment periods separated by a break to allow one menstruation to occur. Efficacy and safety will be compared with that of ulipristal acetate (5 mg daily) and placebo. Patients randomized to receive placebo for 12 weeks will also be given active treatment for 12 weeks. The primary measure of efficacy will be amenorrhoea rate; secondary measures include time to normalized menstrual bleeding and percentage change in UF volume. Endometrial changes will be monitored throughout the study. Discussion: The placebo- and active comparator-controlled trial ASTEROID 2 is the first study to evaluate systematically the efficacy and safety of different treatment regimens of PRMs in women with UFs. The findings of this study will direct the planning of future clinical trials of vilaprisan. © 2017 Bayer AG. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http:// creativecommons.org/licenses/by-nc-nd/4.0/).
VytisknoutZobrazeno: 26. 4. 2024 19:59