LCT) (PINKSHEETS: LVCLY) today announced new
positive 6 month interim results from the Phase I/IIa clinical trial of
DiabeCell® for the treatment of type 1 diabetes at the International
Diabetes Federation (IDF) Congress in Wellington, New Zealand and the NZBio
Conference in Auckland, New Zealand.
Professor Bob Elliott, Medical Director of LCT at the IDF Congress and Dr.
Paul Tan, CEO, at the NZBio Conference, reported that four insulin
dependent patients have received DiabeCell® implants with no remarkable
adverse events. Two of the patients have completed 6 months observation and
maintained significant prolonged clinical benefit.
"Early results from the trial of DiabeCell® at the lowest dose believed
to produce measurable outcomes, have demonstrated that DiabeCell® was
functional at 6 months, and that implantation significantly reduced the
need for additional administration of insulin more than the anticipated
maximum of 25%," said Professor Elliott.
"There is no doubt that a reduction in the level of exogenously
administered insulin is beneficial to people with type 1 diabetes. The
preliminary results are early and unlike adult islets, neonatal islets take
time to mature and delayed benefit can still be expected."
Professor Elliott continued "These remarkable clinical outcomes have
exceeded our expectations. We expect that higher doses of DiabeCell® will
support greater reductions in the insulin needs of patients."
Summary of 6 Month Follow-up Results
-- Four type 1 diabetes patients have been implanted according to the
approved trial protocol with a low dose of DiabeCell® and one of the four
has received a scheduled second implant six months after the initial
-- The first two patients have shown significantly reduced need for
exogenously administered insulin. One male patient's daily insulin
requirement was reduced by 40% over a 6-month period, and a female
patient's need for exogenous insulin was reduced 100% during a 5-month
period before she resumed daily insulin on medical advice to attain better
blood glucose control and insulin dosage reduction of 82% was maintained at
6 months follow up.
-- Implanted microencapsulated cells retrieved from a patient at the time
of the second implant showed that the microencapsulated cells were intact
and contained viable cells. There was no evidence of capsule damage by the
immune system, even though no immunosuppressive drugs were administered in
the DiabeCell® protocol in contrast with the need for immunosuppression
when human islet cells are transplanted using the Edmonton protocol.
-- At 12 weeks after the second implant the daily insulin requirement was
maintained at 40 -47% of the pre-implant requirement with stable glucose
-- The third patient required an increased daily dose of insulin soon
after the first implant to cope with a stressful personal social problem
unrelated to the implant procedure. This patient has not completed 6 months
follow-up and insulin requirement was unchanged at 8 weeks post implant.
-- The fourth patient received her first implant in February 2008 and her
daily insulin requirement was reduced by 10% at only 4 weeks post implant.
-- Results from the first tests for potential porcine endogenous
retroviral infections were negative for all 4 implant recipients
About the trial
-- The trial is under way in Moscow and is intended to enroll a total
of six patients having type 1 diabetes who have given informed
consent for their participation
-- The trial is being monitored by a U.S.-based contract research
-- Patients receive one implantation of DiabeCell® at the lowest
dose anticipated to demonstrate a measureable improvement in
glucose control and need for insulin (among other parameters) at
the commencement of the treatment and again following an additional
implant six months later
-- The following parameters are being measured pre- and post-implant:
-- Daily insulin dose
-- Continuous glucose monitoring
-- Haemoglobin A1c (to indicate average blood glucose over a two-
-- C-peptide in blood (a measure of insulin production) after a
-- Frequency of episodes of low blood glucose
-- Patient satisfaction
APPENDIX - Further Information:
Trial Name: A Phase I/IIA, Open-Label Investigation of the Safety and
Effectiveness of DiabeCell® (Immunoprotected alginate-encapsulated)
Porcine Islets for Xenotransplantation in Patients with Type 1 Diabetes.
Updated Protocol LCT/DIA-07R.
Trial centre details:
-- Sklifosovsky Institute
-- Clinician - Professor Andrej Guljaev, surgeon, Chief of Innovative
Surgical Technology Department.
-- Professor Anatolij Panov, Director of Institute of BioMedical Problems
-- Geny Research Group (US) - Contract Research Organization
Clinical Trial Protocol:
As of 31 March 2008, 6th month follow-up interim report of evaluable data:
Four adult subjects have received implants and one had had a second
-- The human clinical trial of DiabeCell® in Russia has approval to
include six Type 1 (insulin-dependent) diabetics in two stages. Subjects
are over 21 years old to 65 years of age. The candidates have had type 1
diabetes for at least 5 years with no other complications and provide full
consent for follow-up monitoring. The patients received an initial
transplant (a simple injection of encapsulated islets into the peritoneal
cavity of the patient) followed by a second transplant six months later.
The first transplant dose was equivalent to 5,000 IEQ (islet
equivalents/kg). The second transplant was a further 5,000 IEQ's. The
procedure was minimally invasive and administered into the abdomen through
Primary Safety Endpoints
-- One patient had a transient fever following the first implant.
-- Two patients had transient non-specific upper respiratory symptoms one
at 2 weeks and the other at 12 weeks after the first implant.
-- No perioperative reactions were reported. Laparoscopic examination at
the second implant in one patient showed no local tissue reactions to
-- Results from the first tests for porcine endogenous retroviral
infections are negative in all implant recipients
Report on Endpoints to follow are:
-- Occurrence of hypoglycaemic episodes in the post-transplant period in
comparison with those occurring during the 8-week run-in period.
-- Occurrence of perioperative reactions (e.g. wound infections, local
tissue reactions to the alginate microcapsules at the time of
-- Occurrence of other adverse events or serious adverse events.
-- Abnormal laboratory test results, physical examination findings, or
-- Psychological impact (as assessed by the ADDQoL quality-of-life
-- Clinical and laboratory evidence of xenogeneic infection in transplant
recipients via regular monitoring at predefined time points (ongoing).
-- Clinical and laboratory evidence of xenogeneic infection in
partners/close contacts of the transplant recipients (ongoing).
Primary Efficacy Endpoint
For two patients completing 6 months follow-up, insulin requirement was
adjusted over the 6-month post-transplant period to maintain control of
glucose metabolism at or below the target of HbA1c at 7%.
Secondary efficacy endpoints include:
For both patients completing 6 month follow-up the reduction in average
daily insulin requirement exceeded expectation of 25% for the first dose
and was at least 40% and 75% and this was maintained.
Report on Endpoints to follow are:
-- Glucose lability assessed using 72-hour continuous glucose monitoring
(CGMS®, Medtronic Minimed, Northridge, CA) at 3, 6 and 12 months post-
transplant in comparison with baseline, reported as standard deviation of
glucose values at these times (Paty et al. 2006).
-- Reductions in hypoglycemia and nocturnal hypoglycemia, as assessed by
a composite hypoglycaemic score (HYPO score) over the 12-month post-
transplant period compared with baseline (Ryan et al 2004). Patients will
be asked to record the frequency, severity and degree of unawareness of the
hypoglycaemia on a scoring sheet.
-- Reductions in the average daily insulin dose of > 25% unaccompanied by
objective evidence of deterioration of diabetes control at 6 and 12 months
post-transplant compared with baseline, as measured by regular 7-point
blood glucose profiles and monthly HbA1C levels, in the absence of evidence
of major weight loss ( > 10T) or ketoacidosis.
-- Changes in endogenous insulin secretion as determined by the plasma C-
peptide response to a Sustacal Meal at 3, 6 and 12 months post-transplant
compared with baseline. Pre-transplant this test is expected to confirm a
low human C-peptide level; after the xenotransplant, the test should
detect porcine C-peptide/insulin.
-- Quality of life changes, as assessed by the ADDQoL quality-of-life
questionnaire (Appendix 2), at 6 and 12 months post-transplant compared
Scientific papers relating to DiabeCell® are available for download on
the LCT website at www.lctglobal.com/scientificarticles.php
About Living Cell Technologies: www.lctglobal.com
Living Cell is developing cell-based products to treat life threatening
human diseases. The
Company owns a bio-certified pig herd that it uses as a source of cells for
treating diabetes and neurological disorders. For patients .having type 1
diabetes, the Company implants micro-encapsulated islet cells so that
near-normal blood glucose levels may be achieved without the need for
administration of insulin or at significantly reduced levels. The company
entered clinical trials for its diabetes product in 2007. The Company is
developing treatments for Huntington's disease and other neurological
disorders that involve implantation of micro-encapsulated choroid plexus
cells to deliver beneficial proteins and neurotrophic factors to the brain.
Living Cell's technology has the potential for allowing healthy living
cells to be injected into patients to replace or repair damaged tissue
without requiring the use of immunosuppressive drugs to prevent rejection.
Living Cell also is developing medical-grade porcine-derived products for
the repair and replacement of damaged tissues, as well as for research and
other purposes. The changes in this paragraph reflect that the company
only is developing or might develop certain products, and is not
manufacturing or selling any products other than DiabeCell
This document contains certain forward-looking statements, relating to
LCT's business, which can
be identified by the use of forward-looking terminology such as
"promising," "plans," "anticipated," "will," "project," "believe,"
"forecast," "expected," "estimated," "targeting," "aiming," "set to,"
"potential," "seeking to," "goal," "could provide," "intends," "is being
developed," "could be," "on track," or similar expressions, or by express
or implied discussions regarding potential filings or marketing approvals,
or potential future sales of product candidates. Such forward-looking
statements involve known and unknown risks, uncertainties and other factors
that may cause actual results to be materially different from any future
results, performance or achievements expressed or implied by such
statements. There can be no assurance that any existing or future
regulatory filings will satisfy the FDA's and other health authorities'
requirements regarding any one or more product candidates nor can there be
any assurance that such product candidates will be approved by any health
authorities for sale in any market or that they will reach any particular
level of sales. In particular, management's expectations regarding the
approval and commercialization of the product candidates could be affected
by, among other things, unexpected clinical trial results, including
additional analysis of existing clinical data, and new clinical data;
unexpected regulatory actions or delays, or government regulation
generally; our ability to obtain or maintain patent or other proprietary
intellectual property protection; competition in general; government,
industry, and general public pricing pressures; and additional factors that
involve significant risks and uncertainties about our products, product
candidates, financial results and business prospects. Should one or more of
these risks or uncertainties materialize, or should underlying assumptions
prove incorrect, actual results may vary materially from those described
herein as anticipated, believed, estimated or expected. LCT is providing
this information as of March 31, 2008, and does not assume any obligation
to update any forward-looking statements contained in this document as a
result of new information, future events or developments or otherwise.