Can-Fite BioPharma To Initiate Phase II Clinical Trial With CF101 For The Treatment Of Glaucoma

Main Category: Eye Health / Blindness
Also Included In: Clinical Trials / Drug Trials
Article Date: 16 Dec 2009 - 11:00 PDT

email icon email to a friend   printer icon printer friendly   write icon opinions  

Current Article Ratings:

Patient / Public:2 stars

2 (1 votes)

Healthcare Prof:5 stars

5 (1 votes)


Can-Fite BioPharma (TASE:CFBI), a biotechnology company traded on the Tel Aviv Stock Exchange, announced on December 13 the initiation of the regulatory process for a Glaucoma Phase II clinical study in Israel. Leading Medical Centers in Israel will enroll 44 patients with Ocular Hypertension or Glaucoma for the first segment of the trial, who will be treated for 16 weeks with CF101 or placebo. The study will be expanded by up to an additional 88 patients upon successful conclusion of an interim analysis of the first segment. The study protocol was developed with the assistance of Dr. Paul Kaufman, a noted glaucoma researcher at the University of Wisconsin. The study will investigate the efficacy of CF101, as manifest by a decrease in intraocular pressure, as well as the safety of CF101 in this population.

The rationale for the conduct of this study is based on unexpected positive findings from the recently concluded Phase II study in Dry Eye, demonstrating a decrease in the intraocular pressure in patients who were treated with CF101.

Glaucoma is one of the leading causes for blindness and currently about 90 million patients worldwide are affected by the disease. The main treatments today consist of eye drops, which are not easy for patients to use regularly and thus raise compliance challenges. Therefore, there is a market need for a systemic, orally administered drug such as CF101. The market size today is $5.5 Billion and is estimated to grow to around $8.4 Billion in 2012.

Can-Fite announced recently that it retained Plexus Ventures, a global pharmaceutical business development consultancy, to assist with the identification of a partner with the necessary expertise and the appropriate organization to support the clinical development and commercialization of CF101 in the United States, Europe and other markets. CF101 is already licensed out in Japan and South Korea.

Source
Can-Fite BioPharma

Article adapted by Medical News Today from original press release.
Visit our eye health / blindness section for the latest news on this subject.
There are no references listed for this article.
Please use one of the following formats to cite this article in your essay, paper or report:

MLA
Can-Fite BioPharma. "Can-Fite BioPharma To Initiate Phase II Clinical Trial With CF101 For The Treatment Of Glaucoma." Medical News Today. MediLexicon, Intl., 16 Dec. 2009. Web.
13 Feb. 2012. <http://www.medicalnewstoday.com/releases/174224.php>

APA
Can-Fite BioPharma. (2009, December 16). "Can-Fite BioPharma To Initiate Phase II Clinical Trial With CF101 For The Treatment Of Glaucoma." Medical News Today. Retrieved from
http://www.medicalnewstoday.com/releases/174224.php.

Please note: If no author information is provided, the source is cited instead.


Eye Health / Blindness

Most Popular Articles



Follow Our Eye Health News On Twitter

Follow Us On Twitter
Get the latest news for this category delivered straight to your Twitter account. Simply visit our Eye Health / Blindness Twitter account and select the 'follow' option.



View list of all 'What Is...' articles »