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Spots Global Cancer Trial Database for Efficacy and Safety Study of M200(Volociximab in Combination With Liposomal Doxorubicin)

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Trial Identification

Brief Title: Efficacy and Safety Study of M200(Volociximab in Combination With Liposomal Doxorubicin)

Official Title: A Phase 1/2, Open-Label, Adaptive, Randomized Study of Liposomal Doxorubicin With or Without M200 (Volociximab) for the Treatment of Subjects With Advanced Epithelial Ovarian Cancer or Primary Peritoneal Cancer That Have Relapsed After Prior Therapy With a Platinum/Taxane-Based Chemotherapy

Study ID: NCT00635193

Study Description

Brief Summary: This is an open-label study of liposomal doxorubicin with or without volociximab for the treatment of subjects with advanced epithelial ovarian cancer or primary peritoneal cancer relapsed after prior therapy with Plat/Taxane-based chemo. Volociximab is an anti-angiogenic integrin inhibitor being developed for the treatment of solid tumors. Preclinical data with a surrogate volociximab antibody administered as monotherapy indicate encouraging efficacy in terms of tumor reduction and anti-angiogenic effects in mouse ovarian cancer xenograft models. In clinical studies, volociximab has been evaluated in several solid tumor types, including pancreatic, renal, and melanoma, with many subjects who entered the studies with progressive disease remaining progression-free for several months. In all studies in solid tumors, volociximab has shown a favorable safety profile when administered at 10 mg/kg q2wks and more recently at 15 mg/kg qwk. A study of volociximab in combination with liposomal doxorubicin in subjects with ovarian cancer or primary peritoneal cancer who have relapsed after prior platin/taxane therapies is warranted to further evaluate the drug's efficacy and safety. The investigators have thus far activated stage 2 of this study at 11/25 sites. Worldwide, the study aims to enroll 150 subjects.

Detailed Description: This is an open-label study of liposomal doxorubicin with or without volociximab for the treatment of subjects with advanced epithelial ovarian cancer or primary peritoneal cancer relapsed after prior therapy with Plat/Taxane-based chemo. Volociximab is an anti-angiogenic integrin inhibitor being developed for the treatment of solid tumors. Preclinical data with a surrogate volociximab antibody administered as monotherapy indicate encouraging efficacy in terms of tumor reduction and anti-angiogenic effects in mouse ovarian cancer xenograft models. In clinical studies, volociximab has been evaluated in several solid tumor types, including pancreatic, renal, and melanoma, with many subjects who entered the studies with progressive disease remaining progression-free for several months.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

Site Reference ID/Investigator# 75281, Anaheim, California, United States

Site Reference ID/Investigator# 75275, Redondo Beach, California, United States

Site Reference ID/Investigator# 75296, Sunrise, Florida, United States

Site Reference ID/Investigator# 75299, Atlanta, Georgia, United States

Site Reference ID/Investigator# 75300, Savannah, Georgia, United States

Site Reference ID/Investigator# 75301, Hinsdale, Illinois, United States

Site Reference ID/Investigator# 75274, Baltimore, Maryland, United States

Site Reference ID/Investigator# 75294, Jackson City, Missouri, United States

Site Reference ID/Investigator# 75279, Oklahoma City, Oklahoma, United States

Site Reference ID/Investigator# 75295, Corpus Christi, Texas, United States

Site Reference ID/Investigator# 75280, Dallas, Texas, United States

Site Reference ID/Investigator# 75297, Danville, Virginia, United States

Site Reference ID/Investigator# 75298, Williamsburg, Virginia, United States

Site Reference ID/Investigator# 75278, Green Bay, Wisconsin, United States

Site Reference ID/Investigator# 75334, Toorak Gardens, , Australia

Site Reference ID/Investigator# 75335, Woodville South, , Australia

Site Reference ID/Investigator# 75337, Antwerp, , Belgium

Site Reference ID/Investigator# 75336, Brussels, , Belgium

Site Reference ID/Investigator# 75338, Leuven, , Belgium

Site Reference ID/Investigator# 75415, Milan, , Italy

Site Reference ID/Investigator# 75333, Milan, , Italy

Site Reference ID/Investigator# 75344, Bialystok, , Poland

Site Reference ID/Investigator# 75339, Krakow, , Poland

Site Reference ID/Investigator# 75341, Lublin, , Poland

Site Reference ID/Investigator# 75342, Poznan, , Poland

Site Reference ID/Investigator# 75343, Poznan, , Poland

Site Reference ID/Investigator# 75345, Szczecin, , Poland

Site Reference ID/Investigator# 75340, Wroclaw, , Poland

Site Reference ID/Investigator# 75346, Moscow, , Russian Federation

Site Reference ID/Investigator# 75348, Moscow, , Russian Federation

Site Reference ID/Investigator# 75347, St. Petersburg, , Russian Federation

Site Reference ID/Investigator# 75349, Barcelona, , Spain

Site Reference ID/Investigator# 75351, Barcelona, , Spain

Site Reference ID/Investigator# 75352, Barcelona, , Spain

Site Reference ID/Investigator# 75350, Girona, , Spain

Site Reference ID/Investigator# 75353, Madrid, , Spain

Site Reference ID/Investigator# 75354, Stockholm, , Sweden

Site Reference ID/Investigator# 75355, Umea, , Sweden

Site Reference ID/Investigator# 75416, Bellinzona, , Switzerland

Contact Details

Name: Mihail Obrocea, MD

Affiliation: AbbVie

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

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