March 01, 2005
1 min read
Save

Significant clinical benefit of TTT seen in subset of patients in CNV trial

You've successfully added to your alerts. You will receive an email when new content is published.

Click Here to Manage Email Alerts

We were unable to process your request. Please try again later. If you continue to have this issue please contact customerservice@slackinc.com.

MOUNTAIN VIEW, Calif. — A subset of patients in a trial of transpupillary thermotherapy for the treatment of wet age-related macular degeneration showed a significant clinical benefit when compared with placebo, according to a press release from Iridex.

The subset consisted of patients who had a visual acuity of 20/100 or worse; 77 patients were in the test group and 39 were given sham treatment. At the 18-month follow-up, 60 patients' data was available for analysis. At 18 months, visual acuity in 22% (13/60) of the treated eyes improved by one or more Snellen lines, compared with none of the eyes in the sham treatment group. Furthermore, TTT-treated eyes on average lost two lines of visual acuity at 18 months, while sham-treated eyes lost four lines. Both differences were statistically significant, the company stated in a press release.

The trial, known as TTT4CNV, was a multicenter, prospective, double-masked, placebo-controlled study conducted at 22 centers in the United States. The study randomized eyes with subfoveal occult choroidal neovascular (CNV) membranes of 3 mm diameter or smaller and VA between 20/50 and 20/400 to transpupillary thermotherapy or sham treatment.

Transpupillary thermotherapy “clearly benefits patients with vision that is 20/100 or worse,” said Elias Reichel, MD, according to the Iridex press release. “With the TTT4CNV clinical trial, about 42% of the patients enrolled had baseline vision of 20/100 or worse. Remarkably, at 18 months, one-fifth of treated patients showed some improvement in vision compared to their vision prior to the TTT treatment.”