Oxford Pharmascience Group PLC MHRA Advice on OXPzeroT Ibuprofen OTC Opportunity (3946S)
02 Octubre 2017 - 4:15AM
UK Regulatory
TIDMOXP
RNS Number : 3946S
Oxford Pharmascience Group PLC
02 October 2017
2 October 2017
Oxford Pharmascience Group plc
("Oxford Pharmascience" or the "Company")
MHRA Advice on OXPzero(TM) Ibuprofen OTC Opportunity
Oxford Pharmascience, the specialty pharmaceutical company that
redevelops medicines to make them better, safer and easier to take,
today announces it has received written advice from the MHRA (UK
regulatory authority) regarding a possible application for
marketing authorisation for an OTC product under development
containing OXPzero(TM) Ibuprofen. Key points from the advice
are:
-- The application can be submitted as a hybrid application
(under article 10(3) of Directive 2001/83/EC), bridging to the
well-established safety and efficacy of the reference product.
-- The MHRA did not consider the OXPzero(TM) Ibuprofen product
to be bioequivalent to the reference due to faster Tmax (time to
maximum concentration) compared to the reference product.
-- While the earlier Tmax of the OXPzero(TM) Ibuprofen product
is believed by the Company to be advantageous for onset of
efficacy, due to the Tmax not sufficiently matching reference, the
MHRA requires additional clinical data on safety and efficacy to
support the marketing authorisation application.
Following receipt of the latest regulatory feedback from the
MHRA, the Company is pleased to note that the hybrid application
route can be used to register the product. However, the requirement
for further clinical safety and efficacy data (in the absence of
bioequivalence) may affect the economic viability of the
programme.
A decision is required regarding whether to invest in the above
additional clinical work or to embark on other further development
to match the reference within the required range for
bioequivalence. Before deciding how best to take the programme
forward, the Company will seek further regulatory agency advice in
different jurisdictions and is now in the process of preparing for
scientific advice meetings with the MPA (Swedish regulatory agency)
and the US FDA. Additionally, the Company may also seek advice from
other EU agencies if considered necessary.
At present the Company has suspended development activities
while the Board concludes a strategic review to assess how to best
realise the value of the Company's assets at the present time
and/or how to best obtain better value from these assets over time.
The Company will confirm the Board's findings as soon as
conclusions have been reached.
Marcelo Bravo, Chief Executive Officer of Oxford Pharmascience,
commented:
"We have received very positive consumer research results on our
lead OTC programme, but need to better understand the regulatory
pathway to product approval in key markets before proceeding with
further development. The MHRA advice has been very informative to
us as we map out our portfolio product development strategies and
we look forward to receiving advice from other regulatory agencies
in the coming months."
For further information please contact:
Oxford Pharmascience Group Plc
Marcelo Bravo, Chief Executive +44 20 7554 5875
N+1 Singer (Nominated Adviser & Broker)
Aubrey Powell/Lauren Kettle +44 20 7496 3000
About Oxford Pharmascience Group Plc
Oxford Pharmascience Group Plc uses a range of proprietary
technology platforms to re-develop existing medicines to make them
better, safer or easier to take. The Company does not manufacture
or sell its own pharmaceutical products direct to consumers, but
instead seeks to license its technologies and dossiers to a network
of partners, mainly leading pharmaceutical companies with Rx
(prescription) and OTC (over the counter) branded portfolios.
Oxford Pharmascience Group Plc focuses on existing medicines
that are proven to be safe and effective but nevertheless still
have associated issues and side effects often affecting compliance.
By working with such medicines, the Company is able to develop new
innovative products for a fraction of the cost, in much quicker
timescales and without the high risk of failure associated with
developing new drugs.
This information is provided by RNS
The company news service from the London Stock Exchange
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