Data from Final Cohort of Patients in Patrys Multiple Myeloma Clinical Trial
November 29 2013 - 12:51AM
Business Wire
- PAT-SM6 clinical trial data from all
4 cohorts to be presented at prestigious American Society of
Hematology conference
- From 11 currently evaluable
patients, 4 (36%) experienced stable disease post treatment with
PAT-SM6
- No serious adverse events
reported
- Preparing to initiate a combination
study with Patrys’ PAT-SM6 and Onyx Pharmaceuticals’
carfilzomib
Patrys Limited (ASX:PAB), a clinical stage biotechnology
company has announced that updated results from its PAT-SM6 Phase
I/IIa clinical trial in multiple myeloma (MM) will be presented at
the 55th American Society of Hematology (ASH) Annual Meeting in New
Orleans, LA on 7- 10 December 2013.
To date eleven out of a total of twelve patients are currently
available for response evaluation, including two out of three from
the 4th and final treatment group. The 12th patient is not yet
evaluable. This final group received four doses of PAT-SM6 at
6mg/kg/dose as per the protocol. To date, four out of eleven of the
patients (36%) with end-stage, multi-resistant MM have shown
evidence of stable disease according to the International Myeloma
Working Group criteria.
The eleven patients (9 male and 2 female, median age 71 years)
had, on average, received five prior lines of therapy including
autologous stem cell transplantation and other novel marketed
compounds including Velcade and Revlimid. Therapeutic options for
such patients are usually limited to clinical trials and their
median overall survival is around nine months.
All of the eleven evaluable patients tolerated PAT-SM6 very
well. There were no drug-related serious adverse events and no
dose-limiting toxicities.
These updated results will be presented by lead clinical
investigator Dr. Leo Rasche from the Department of Haematology and
Oncology, University Hospital of Würzburg. His presentation is
titled “A monoclonal IgM antibody with specificity to heat shock
protein GRP78/BIP shows anti-myeloma activity in vitro and in vivo,
synergy in combination with Lenalidomide and safety in a pilot
Phase I study”.
“Our trial with PAT-SM6 has produced some very exciting clinical
data and it is particularly encouraging to see four patients, with
end-stage multiple myeloma, respond so positively to treatment with
this novel antibody,” commented Patrys’ CEO, Dr. Marie Roskrow.
“These clinical data, in conjunction with an extensive preclinical
package, have positioned our lead product, PAT-SM6, for the next
clinical trial to be sponsored by Onyx Pharmaceuticals, a
subsidiary of Amgen”.
Patrys Limited:Dr. Marie
RoskrowChief Executive OfficerP: +61 3 9670
3273info@patrys.comorPatrys IR:Rebecca
WilsonBuchan ConsultingP: 0417 382
391rwilson@buchanwe.com.auorPatrys
Media:Kellie HanrickBuchan ConsultingP: +61 3 9866
4722khanrick@buchanwe.com.au
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