A Phase I, Open Label, Dose Escalation Study of the VEGF-C Human Monoclonal Antibody VGX-100 Administered by Intravenous Infusion Alone and Co-administered With Bevacizumab in Adult Subjects With Advanced or Metastatic Solid Tumors

This is a non-randomized, multi-dose, first-in-human, multicenter, two arm (Arm A: VGX-100 alone; Arm B: VGX-100 co-administered with bevacizumab), open label, dose escalation study in subjects with advanced or metastatic solid tumors. The study is aimed at evaluating the safety and establishing the recommended dose of the VEGF-C human monoclonal antibody VGX-100 when administered alone or in combination with bevacizumab.

Start Date29 Dec 2011

Sponsor / Collaborator

Circadian Technologies, Inc.

100 Clinical Results associated with VGX-100

100 Translational Medicine associated with VGX-100

100 Patents (Medical) associated with VGX-100

Literatures (Medical) associated with VGX-100

03 May 2016·Expert Opinion on Investigational DrugsQ2 · MEDICINE

Novel anti-angiogenic therapeutic strategies in colorectal cancer

Q2 · MEDICINE

Review

Author: Tampellini, M ; Sonetto, C ; Scagliotti, G V

INTRODUCTIONAnti-angiogenetic agents are currently the standard of care in metastatic CRC patients. Bevacizumab, aflibercept, regorafenib and recently ramucirumab have significantly improved both progression-free and overall survival in different lines of treatment. Since bevacizumab's approval, a number of novel anti-VEGF agents have been tested in preclinical and clinical models.AREAS COVEREDThis review is focused on the most recent clinical results of novel agents targeting VEGF and its receptors with a major focus on those investigated recently in clinical trials.EXPERT OPINIONIn the last 15 years, a number of new anti-angiogenetic agents have been tested. Unfortunately, most of them have demonstrated unacceptable toxicities or failed to show activity. When tested as single agents, encouraging preliminary results were reported with fruquintinib, famitinib, and nintedanib. Interesting novel mechanisms of action are also being explored: VGX-100 is a monoclonal antibody (mAb) which binds to VEGF-C, inhibiting activation of VEGFR-2 and VEGFR-3 when combined with bevacizumab; tanibirumab is a mAb which binds to VEGFR-2 and vanucizumab is a bispecific mAb binding both to VEGF-A and Angiopoietin-2. Data about the combination of these agents with chemotherapy are very encouraging, even though preliminary. However, the definition of specific predictive biomarkers remains a priority.

100 Deals associated with VGX-100

R&D Status

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Indication	Highest Phase	Country/Location	Organization	Date
Advanced Malignant Solid Neoplasm	Phase 2	US	Circadian Technologies, Inc.	29 Dec 2011
Eye Diseases	Phase 2	-	Vegenics Pty Ltd.	-
Eye Diseases	Phase 2	-	Ceres Oncology	-
Solid tumor	Phase 2	-	Opthea Ltd.	-

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Study	Phase	Population	Analyzed Enrollment	Group	Results	Evaluation	Publication Date


NCT01514123 (Literature) Manual	Phase 1	Advanced Malignant Solid Neoplasm	43	VGX-100 + bevacizumab	(joeolgigbn) = the most common grade 1-2 toxicities were fatigue, rash, nausea, anorexia and hypertension. vaqmchuuqb (dogitqlojp ) View more	Positive	20 May 2014
				VGX-100

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