Completes Phase II Study Design for CF102 in the Treatment of NASH/NAFLD

Completes Phase II Study Design for CF102 in the Treatment of NASH/NAFLD

TIKVA, Israel, July 25, 2016 -- Can-Fite BioPharma Ltd. (NYSE MKT: CANF) (TASE:CFBI), a biotechnology company with a pipeline

of proprietary small molecule drugs being developed to treat inflammatory diseases, cancer and sexual dysfunction, announced today

that it completed the protocol design for its upcoming Phase II trial of its drug candidate CF102 in the treatment of non-alcoholic

fatty liver disease (NAFLD), the precursor to non-alcoholic steatohepatitis (NASH).

is characterized by excess fat accumulation in the form of triglycerides (steatosis) in the liver. According to a recent study

published in Hepatology, an estimated 25% of the population in the U.S. has NAFLD, with a higher prevalence in people with type

II diabetes. Incidence is increasing based on rising obesity rates. NAFLD includes a range of liver diseases, with NASH being

the more advanced form, manifesting as hepatic injury and inflammation. According to the NIH, the incidence of NASH in the U.S.

is believed to affect 2-5% of the population. The spectrum of NAFLDs resembles alcoholic liver disease; however, they occur in

people who drink little or no alcohol. If untreated, NASH can lead to cirrhosis and liver cancer.

2025, Deutsche Bank estimates the addressable pharmaceutical market for NASH will reach $35-40 billion in size. As of today, while

there are several companies developing drugs to treat NAFLD/NASH that are in preclinical and clinical development, no specific

U.S. Food and Drug Administration (FDA) approved treatment exists.

to the study design, Can-Fite's Phase II study, which was designed by world renowned Key Opinion Leaders in the field of

liver diseases, will be a multicenter, randomized, double-blinded, placebo-controlled, dose-finding study of the efficacy and

safety of CF102 in the treatment of Non-Alcoholic Fatty Liver Disease (NAFLD). The study will enroll approximately 75 patients

and will have three arms, including two different dosages of CF102 and a placebo, given via oral tablets twice daily. The study's

primary endpoints will be percent change from baseline in liver triglyceride (fat) concentration measured by nuclear magnetic

resonance spectroscopy (NMRS) and safety. Secondary endpoints include the effects of CF102 on metabolic abnormalities in patients

with NAFLD; the effects of CF102 on relevant NAFLD related biomarkers; and an assessment of the pharmacokinetics (PK) of CF102

in patients with NAFLD. The A3 adenosine receptor (A3AR) biomarker will be evaluated prior to treatment and its correlation to

patients' response to the drug will be analyzed upon study conclusion. The study will be conducted in leading medical centers

in Israel and is expected to be submitted to IRBs in the fourth quarter of this year.

are very pleased the Phase II study design for the indication of NAFLD/NASH is completed and we look forward to commencing this

important study. Based on the good safety data we have on CF102 from our current Phase II trial in liver cancer, its anti-inflammatory

as well as liver protective profile, and the positive pre-clinical data in NASH models, we believe patients with NAFLD may benefit

from CF102," stated Can-Fite CEO Pnina Fishman.

is currently being evaluated in a Phase II study for the treatment of hepatocellular carcinoma (HCC). Recent preclinical studies

of CF102 revealed its capability to improve liver pathology in a NAFLD animal model of NASH including data showing a statistically

significant reduction in NAFLD activity score compared to placebo.

is a small orally bioavailable drug that binds with high affinity and selectivity to the A3 adenosine receptor (A3AR). A3AR is

highly expressed in tumor cells whereas low expression is found in normal cells. This differential effect accounts for the excellent

safety profile of the drug. In Can-Fite's pre-clinical and clinical studies, CF102 has demonstrated a robust anti-tumor effect

via deregulation of the Wnt signaling pathway, resulting in apoptosis of liver cancer cells.

Can-Fite BioPharma Ltd.

BioPharma Ltd. (NYSE MKT: CANF) (TASE: CFBI) is an advanced clinical stage drug development Company with a platform technology

that is designed to address multi-billion dollar markets in the treatment of cancer, inflammatory disease and sexual dysfunction.

The Company's lead drug candidate, Piclidenoson, is scheduled to enter Phase III trials in 2016 for two indications, rheumatoid

arthritis and psoriasis. The rheumatoid arthritis Phase III protocol has recently been agreed with EMA. Can-Fite's liver cancer

drug CF102 is in Phase II trials for patients with liver cancer and is slated to enter Phase II for the treatment of non-alcoholic

steatohepatitis (NASH). CF102 has been granted Orphan Drug Designation in the U.S. and Europe and Fast Track Designation as a

second line treatment for hepatocellular carcinoma by the U.S. Food and Drug Administration. CF102 has also shown proof of concept

to potentially treat other cancers including colon, prostate, and melanoma. CF602, the Company's third drug candidate, has shown

efficacy in the treatment of erectile dysfunction in preclinical studies and is being prepared for an IND submission to the FDA

and a Phase I trial. These drugs have an excellent safety profile with experience in over 1,000 patients in clinical studies to

date. For more information please visit: www.can-fite.com.

press release may contain forward-looking statements, about Can-Fite's expectations, beliefs or intentions regarding, among other

things, its product development efforts, business, financial condition, results of operations, strategies or prospects. In addition,

from time to time, Can-Fite or its representatives have made or may make forward-looking statements, orally or in writing. Forward-looking

statements can be identified by the use of forward-looking words such as "believe," "expect," "intend,"

"plan," "may," "should" or "anticipate" or their negatives or other variations of these

words or other comparable words or by the fact that these statements do not relate strictly to historical or current matters.

These forward-looking statements may be included in, but are not limited to, various filings made by Can-Fite with the U.S. Securities

and Exchange Commission, press releases or oral statements made by or with the approval of one of Can-Fite's authorized executive

officers. Forward-looking statements relate to anticipated or expected events, activities, trends or results as of the date they

are made. Because forward-looking statements relate to matters that have not yet occurred, these statements are inherently subject

to risks and uncertainties that could cause Can-Fite's actual results to differ materially from any future results expressed or

implied by the forward-looking statements. Many factors could cause Can-Fite's actual activities or results to differ materially

from the activities and results anticipated in such forward-looking statements, including, but not limited to, the factors summarized

in Can-Fite's filings with the SEC and in its periodic filings with the TASE. In addition, Can-Fite operates in an industry sector

where securities values are highly volatile and may be influenced by economic and other factors beyond its control. Can-Fite does

not undertake any obligation to publicly update these forward-looking statements, whether as a result of new information, future

events or otherwise.