Intarcia Therapeutics, Inc. Presents Positive ITCA 650 Phase 2 Study Results as a Late-Breaker at the American Diabetes Association 70th Scientific Sessions

HAYWARD, Calif., June 28 /PRNewswire/ -- Intarcia Therapeutics, Inc. presented today the results of a phase 2 clinical study of ITCA 650 (DUROS® continuous subcutaneous delivery of exenatide) for the treatment of type 2 diabetes as a late-breaker at the Annual Conference of the American Diabetes Association in Orlando, FL (June 25-29, 2010). Results of the phase 2 study demonstrated substantial reductions in HbA1c and body weight during the 12 weeks of treatment with ITCA 650 at both the 20 mcg/day and 40 mcg/day doses.

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The phase 2 study was conducted at 50 centers in the United States and evaluated a 12-week course of two doses of ITCA 650 compared with twice daily injections of exenatide (Byetta®) among 155 type 2 diabetes patients (51-53 patients/arm) on a stable treatment regimen of metformin. The study included three dose arms to which patients were randomized to receive either ITCA 650 at doses of 20 mcg/day or 40 mcg/day, or twice daily injections of exenatide at 5 mcg BID for 4 weeks followed by 10 mcg BID thereafter as indicted in the product label.

Summary of week 12 results

ITCA 650 20 mcg/day

ITCA 650 40 mcg/day

Exenatide injection

Mean baseline HbA1c




Mean week 12 HbA1c




Change from baseline




% HbA1c < 7.0




% HbA1c < 6.5




Mean baseline body weight

93.5 kg

91.5 kg

93.4 kg

Mean % change in body weight at week 12




DUROS continuous delivery of exenatide resulted in a reduced incidence and persistence of treatment-associated nausea. Nausea rates among patients receiving ITCA 650 at 40 mcg/day were similar to those receiving exenatide injections at 10 mcg BID. Nausea rates observed among patients receiving ITCA 650 at 20 mcg/day were lower than patients receiving the same daily dose with BID injections.

The phase 2 study also incorporated a quality of life (QOL) assessment (DM-SAT) completed by each patient prior to initiating treatment and again at treatment week 8. The results of this assessment suggest that patients receiving either dose of ITCA 650 experienced greater improvement in their quality of life compared to patients receiving twice daily injections of exenatide.

ITCA 650 20 mcg/day

ITCA 650 40 mcg/day

Exenatide injection

% improvement in patient-assessed QOL at week 8




Other clinical observations from the phase 2 study include reductions in both LDL-C and systolic blood pressure from baseline. Approximately 92% of patients completed treatment, and discontinuation rates ranged from 5.9% on ITCA 650 at 40 mcg/day to 9.4% on exenatide twice daily injection.

ITCA 650 20 mcg/day

ITCA 650 40 mcg/day

Exenatide injection

Change in LDL-C

-4.8 mg/dL

-5.4 mg/dL

+1.2 mg/dL

Change in systolic blood pressure

-3.6 mmHg

-6.8 mmHg

-4.2 mmHg

"The results of the phase 2 study suggest that ITCA 650 may play an important role in the treatment of type 2 diabetes," said Dr. Robert Cuddihy, MD, Medical Director, International Diabetes Center at Park Nicollet in Minneapolis, MN and a study investigator who presented the results at the ADA meeting. "Compliance is a significant challenge for many patients, and ITCA 650 ensures the delivery of every dose everyday. No other treatment can do that."

In an ongoing 12-week extension phase of the study, patients receiving ITCA 650 were randomized to remain on their current dose or increase their ITCA 650 dose; patients receiving twice daily injections of exenatide were switched to ITCA 650 therapy at one of two doses. The dosing and treatment changes have been well tolerated and the interim week 20 HbA1c results are presented below.

Summary of week 20 interim HbA1c results including 108 patients who have completed 20 weeks of treatment to date:

Week 20

ITCA 650 20 mcg/day

ITCA 650 40 mcg/day

ITCA 650 60 mcg/day

ITCA 650 80 mcg/day

Mean baseline HbA1c





Mean week 20 HbA1c




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