Starpharma creates slow release soluble DEP remdesivir nanoparticle
01 Setembro 2020 - 9:55AM
Business Wire
- DEP® remdesivir has been created to expand the potential
application of remdesivir, by creating a long-acting version which
could be administered subcutaneously rather than by intravenous
infusion in hospital
- DEP® remdesivir is a highly water-soluble nanoparticle
formulation of the antiviral drug remdesivir (Veklury, Gilead) with
improved pharmacokinetics
- Gilead’s antiviral drug, remdesivir, is being utilised for
the treatment of COVID-19
Starpharma (ASX: SPL, OTCQX: SPHRY) today announced it has
applied its novel DEP® drug delivery technology to create a
long‑acting, water soluble version of remdesivir. Remdesivir is an
antiviral drug, currently being developed by Gilead to treat
COVID-19 and has emergency use authorisation from the US Food and
Drug Administration for the treatment of COVID-19 in adults and
children hospitalised with severe disease.
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DEP® remdesivir has >100-fold higher
solubility than remdesivir (Photo: Business Wire)
Remdesivir has broad-spectrum antiviral activity. Current
formulations of remdesivir are required to be administered
intravenously due to the drug’s low solubility, with each infusion
taking up to two hours and requiring daily administration for
either 5 or 10 days.
In contrast, Starpharma’s DEP® remdesivir is a highly
water-soluble nanoparticle formulation of remdesivir with
controlled release properties, which would potentially allow for
less frequent dosing and use in a non-hospital setting, such as
aged-care. The solubility of DEP® remdesivir is 100‑fold higher
than standard remdesivir. The benefit of DEP® remdesivir’s enhanced
aqueous solubility is that it would enable subcutaneous injection
rather than intravenous infusion, allowing for outpatient treatment
and reducing the burden on hospitals.
Dr Jackie Fairley, Starpharma CEO, commented: “Given the limited
treatment options available for COVID-19 patients, Starpharma has
been actively reviewing development programs globally, and
evaluating where Starpharma’s proprietary DEP® technology has
potential to improve delivery, expand use or reduce frequency of
dosing”.
“The ability to deliver remdesivir via a long-acting,
subcutaneous injection has the potential to expand its application
outside hospitals, into settings like aged care, and also
facilitate its use in countries with less developed healthcare
systems. It would also improve patient convenience and reduce the
burden on the healthcare system. We’re pleased to be able to
utilise the DEP® platform to improve the delivery of this important
antiviral medicine”.
“The development of DEP® remdesivir is Starpharma’s 2nd program
addressing COVID-19, and potentially future pandemics. This is
separate to the development of its SPL7013 antiviral nasal spray
for COVID-19, which was detailed in a market update last week”,
added Dr Fairley.
About DEP®
Starpharma’s novel dendrimer-based DEP® platform has broad
commercial applicability in drug delivery by enhancing the
therapeutic utility of drugs through improved solubility, efficacy
and pharmacokinetics, reductions in certain toxicities (e.g. bone
marrow toxicity) and creating a unique intellectual property
position. The novel DEP® platform has shown reproducible advantages
across a wide range of drug classes and can be utilised with both
small molecule drugs, peptides and proteins. The DEP® technology
provides the opportunity to create new intellectual property when
used in conjunction with an existing drug.
For more information on Starpharma’s proprietary DEP® drug
delivery technology visit www.starpharma.com/drug_delivery.
Starpharma has a range of clinical-stage and preclinical stage
DEP® products being developed internally and also with partners.
Starpharma has three DEP® products, DEP® docetaxel, DEP®
cabazitaxel and DEP® irinotecan, which are in phase 2 trials, and
further DEP® assets are progressing through the preclinical
development pipeline. Starpharma’s partnered DEP® programs include
a multiproduct DEP® licence with AstraZeneca, which includes the
development of AZD0466, a Bcl2/xL inhibitor that is currently in a
phase 1 trial in the US. Starpharma also has a research partnership
with leading Chinese Pharmaceutical company, Chase Sun, and other
undisclosed partnerships, including Targeted DEP® partnerships with
world leading ADC companies.
For more information visit www.starpharma.com.
Disclosure
This ASX Announcement was authorised for release by the
Chairman, Mr Rob Thomas.
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version on businesswire.com: https://www.businesswire.com/news/home/20200901005473/en/
Media: WE Communications Rebecca Wilson Mob: +61 417 382
391 rwilson@we-worldwide.com Arthur Chan +61 2 9237 2805
arthurc@we-worldwide.com Starpharma Holdings Limited Dr
Jackie Fairley, Chief Executive Officer Nigel Baade, CFO and
Company Secretary +61 3 8532 2704 investor.relations@starpharma.com
4-6 Southampton Crescent Abbotsford Vic 3067 Tony Eglezos VP
Business Development +61 3 8532 2704
busdev@starpharma.com (Partnering)
Starpharma (ASX:SPL)
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