Reduced Time in Hypoglycemia Demonstrated in Tandem Diabetes Care's Pivotal Trial for the t:slim X2 Insulin Pump with Predictive Low Glucose Suspend Feature; Data to be Presented at ATTD 2018 Conference
The t:slim X2 Insulin Pump with Basal-IQ technology utilizes Dexcom G5® Mobile Continuous Glucose Monitoring (CGM) sensor values to suspend insulin delivery when low blood glucose is predicted and automatically resume insulin delivery when glucose levels begin to rise. Use of the system during a 3-week period at home reduced the number of sensor glucose readings below 70 mg/dL by 31 percent compared to the control period using a standard CGM-integrated t:slim X2 Pump without automated insulin suspension. Importantly, this marked reduction of time spent in low glucose was accomplished without any increase in the rate of hyperglycemia.
"Tandem's t:slim X2 Insulin Pump with Basal-IQ proved easy to use,
reduced time spent in hypoglycemia and improved time in range. These
results are especially impressive given the study participants started
out very well controlled, with a mean hemoglobin A1c of 7.3 percent.
Participants also reported a high level of confidence using the system
without a significant training burden to get started," said
"Reducing the risk of hypoglycemia has been the most requested feature
of automated insulin delivery in our market research, due to the
severity of the complications when left untreated. The data from this
study supports our mission to improve the lives of people with diabetes
through new innovations, such as the t:slim X2 Pump with Basal-IQ
technology," said
About the PROLOG Study
The PROLOG study was a multi-center, randomized crossover clinical trial
comparing two 3-week periods of at-home insulin pump use, one period
using the t:slim X2 Pump with PLGS, and another period using a standard
CGM-integrated t:slim X2 Pump without automated insulin suspension. The
study included 103 participants with type 1 diabetes age 6 to 72 at four
research centers across
About
Forward Looking Statement
This press release contains "forward-looking statements" within the
meaning of Section 27A of the Securities Act of 1933, as amended, and
Section 21E of the Securities Exchange Act of 1934, as amended, that
concern matters that involve risks and uncertainties that could cause
actual results to differ materially from those anticipated or projected
in the forward-looking statements. These forward-looking statements
relate to, among other things, whether the data from the PROLOG study
will be adequate to support a future regulatory filing by Tandem, the
anticipated timing of a PMA submission for the t:slim X2 with BASAL-IQ
and the planned launch of t:slim X2 with BASAL-IQ in the summer of 2018.
These statements are subject to numerous risks and uncertainties,
including the risk that the data from the PROLOG study may not be
adequate to support a future regulatory approval of the t:slim X2 with
BASAL-IQ, that the approval of the t:slim X2 with BASAL-IQ may not occur
when expected or that Tandem may encounter other challenges that may
delay the commercial launch of t:slim X2 with BASAL-IQ, as well as other
risks identified in Tandem's most recent Annual Report on Form 10-K and
Quarterly Reports on Form 10-Q, respectively, and other documents that
we file with the
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Media:
ssabicer@thesabicergroup.com
or
Investors:
smorrison@tandemdiabetes.com
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