Rexahn Pharmaceuticals begins treatment under Phase IIa trial of Supinoxin in metastatic TNBC negative breast cancer patients.
M2 EQUITYBITES-February 24, 2017-Rexahn Pharmaceuticals begins treatment under Phase IIa trial of Supinoxin in metastatic TNBC negative breast cancer patients
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Biopharmaceutical company Rexahn Pharmaceuticals Inc (NYSE MKT:RNN) reported on Thursday the start of dosing of the patient under the Phase IIa clinical study of Supinoxin to evaluate the safety and efficacy of Supinoxin in patients with metastatic TNBC negative breast cancer (TNBC) who have failed prior treatments.
This Phase IIa clinical proof-of-concept study is an open-label evaluation of the safety and efficacy of the company's Supinoxin monotherapy in patients with metastatic triple negative breast cancer who have failed multiple prior chemotherapeutic regimens. The primary endpoint is progression free survival.
As part of the study, the company will recruit an initial ten patients, who will be enrolled at seven study sites in the US. The study can also be extended up to 50 patients, if warranted, based on the data readout from the initial cohort of patients.
The company added that Supinoxin (RX-5902) is an orally administered, potential first-in-class, small molecule modulator of the ?-catenin pathway - a key biological pathway that is activated in tumor cells leading to production of multiple cancer oncogenes and tumor proliferation and metastasis. Supinoxin modulates the pathway through inhibition of the interaction of phosphorylated p68 (a regulatory protein) with ?-catenin.
Triple negative breast cancer (TNBC) refers to any breast cancer that does not express the genes for estrogen receptor (ER), progesterone receptor (PR) or Her2/neu. It is also more aggressive than other types of breast cancer and is more likely to recur.
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|Publication:||M2 EquityBites (EQB)|
|Article Type:||Clinical report|
|Date:||Feb 24, 2017|
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