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AKARI THERAPEUTICS PLC CONSOLIDATED ANNUAL REPORT AND FINANCIAL STATEMENTS FOR THE YEAR ENDED 31 DECEMBER 2018 Registered Number: 05252842 AKARI THERAPEUTICS PLC CONSOLIDATED ANNUAL REPORT AND FINANCIAL STATEMENTS FOR TH

Key Takeaway: AKARI THERAPEUTICS PLC CONSOLIDATED ANNUAL REPORT AND FINANCIAL Registered Number: 05252842 AKARI THERAPEUTICS PLC CONSOLIDATED ANNUAL REPORT AND FINANCIAL FOR THE YEAR ENDED 31 DECEMBER 2018 C ONTENTS Page Officers and professional advisers 1 Directors' report 2 - 3 Strate

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AKARI THERAPEUTICS PLC
CONSOLIDATED ANNUAL REPORT AND FINANCIAL
Registered Number: 05252842
AKARI THERAPEUTICS PLC
CONSOLIDATED ANNUAL REPORT AND FINANCIAL
FOR THE YEAR ENDED 31 DECEMBER 2018
C ONTENTS Page
Officers and professional advisers 1
Directors' report 2 - 3
Strategic Report 4 - 10
Director's Remuneration Report 11-19
Independent Auditors' report to the shareholders of Akari Therapeutics Plc 20-22
Consolidated statement of comprehensive loss 23
Consolidated statement of financial position 24
Parent company statement of financial position 25
Consolidated statement of changes in equity 26
Parent company statement of changes in equity 26
Consolidated statement of cash flows 27
Parent company statement of cash flows 28
Notes to the report and financial statements 29-43
AKARI THERAPEUTICS PLC
OFFICERS AND PROFESSIONAL ADVISERS
FOR THE YEAR ENDED 31 DECEMBER 2018
Directors R Prudo-Chlebosz
C Richardson
J Hill
S Ungar
D Byrne
R Ward (resigned 19 September 2018)
D Williams
D Solomon (resigned 8 May 2018)
M Grissinger
P Feldschreiber
Secretary SLC Corporate Services Limited (resigned 20 August 2018)
Prism Cosec Limited
D Elefant
Registered Office Elder House St George's Business Park
207 Brooklands Road,
Weybridge,
Surrey,
KT13 0TS
Independent Auditors Haysmacintyre LLP
10 Queen Street Place
London
EC4R 1AG
AKARI THERAPEUTICS PLC
FOR THE YEAR ENDED 31 DECEMBER 2018
Unless the context otherwise requires, all
references to "Akari," "we," "us," "our," the "Company", the "Group"
and similar designations refer to Akari Therapeutics, Plc and its subsidiaries. All references to "parent company"
refer to Akari Therapeutics, Plc excluding its subsidiaries.
The directors present their report and the
audited financial statements for the year ended 31 December 2018.
The principal activity of the Group is developing
inhibitors of acute and chronic inflammation, specifically the complement system, the eicosanoid or leukotriene system and the
bioamine system for the treatment of rare and orphan diseases.
The directors who served the company during
the year and up to the date of signing the Annual Report were as follows:
R Ward (resigned 19 September 2018)
D Solomon (resigned 8 May 2018)
SUPPLIER PAYMENT POLICY
It is the Group's policy to agree to
commercial terms with its suppliers prior to purchase of goods or services. The Group negotiates favourable payment terms where
CORPORATE GOVERNANCE
The Group is not required to implement the
provisions of the UK Corporate Governance Code (the "Code").
Regular board meetings are held and the Executive
Directors are heavily involved in the day to day running of the business. The Board of Directors meets regularly and is responsible
for formulating strategy, monitoring financial performance and approving material items of expenditure.
The Group meets its day-to-day working capital
requirements through funding. The Group's forecast and projections, show that at present, the Group has insufficient working
capital to fulfil its current business plan for the next twelve months from the date of approval of the financial statements without
the Group raising additional capital. However, the Group also has the option to revise its plan including reducing the scale of
its operations and pace of development, to reduce discretionary costs to ensure its cost and liabilities are met from existing
working capital resources. Therefore, having reviewed the Group's forecast and projections, and having made appropriate enquiries,
the Directors have a reasonable expectation that the Group has sufficient funding and adequate resources to continue operationally
for at least 12 months from the date of this Annual Report. The Group therefore continues to adopt the going concern basis
for the preparation of the consolidated financial statements.
AKARI THERAPEUTICS PLC
DIRECTORS' REPORT (continued)
FOR THE YEAR ENDED 31 DECEMBER 2018
STATEMENT OF DIRECTORS' RESPONSIBILITIES
The directors are responsible for preparing
the Annual Report and the financial statements in accordance with applicable laws and regulations.
Company law requires the directors to prepare
Group and Parent company financial statements for each financial year. Under that law the directors have elected to prepare the
Group and Parent company financial statements in accordance with International Financial Reporting Standards ("IFRS")
as adopted by the EU. Under company law the directors must not approve the financial statements unless they are satisfied that
they give a true and fair view of the state of affairs of the Group and the Company and the profit or loss of the Group for that
The Group financial statements are required
by law and IFRS as adopted by the EU to present fairly the financial position and performance of the Group; the Companies Act 2006
provides in relation to such financial statements that references in the relevant part of that Act to financial statements giving
a true and fair view are references to their achieving a fair presentation. The Parent company financial statements are required
by law to give a true and fair view of the state of affairs of the Parent company.
In preparing these financial statements the
directors are required to:
The directors are responsible for keeping proper
accounting records which disclose with reasonable accuracy at any time the financial position of the Group and Parent company and
to enable them to ensure that the financial statements comply with the Companies Act 2006 and Article 4 of the IAS Regulation.
They have general responsibility for taking such steps as are reasonably open to safeguard the assets of the Group and Parent company
and to prevent and detect fraud and
other irregularities.
The directors consider that the Annual Report,
taken as a whole, is fair, balanced and understandable and provides the information necessary for shareholders to assess the Group's
performance, business model and strategy.
DISCLOSURE OF INFORMATION TO AUDITORS
So far as each of the directors is aware at
the time the report is approved:
This report was approved by the board on 30
May 2019 and signed on its behalf.
/s/ Clive Richardson
AKARI THERAPEUTICS PLC
FOR THE YEAR ENDED 31 DECEMBER 2018
We are a clinical-stage biopharmaceutical company
focused on developing inhibitors of acute and chronic inflammation, specifically the complement system, the eicosanoid or leukotriene
system and the bioamine system for the treatment of rare and orphan diseases. Each of these systems has scientifically well-supported
causative roles in the diseases being targeted by us. We believe that blocking early mediators of inflammation will prevent initiation
and continual amplification of the processes that cause certain diseases.
Ticks have undergone 300 million years of natural
selection to produce inhibitors that bind tightly to key highly-conserved inflammatory mediators, are generally well tolerated
in humans, and remain fully functional when a host is repeatedly exposed to the molecule. Our molecules are derived from these
Our lead product candidate, nomacopan (Coversin),
which is a second-generation complement inhibitor, acts on complement component-C5, preventing release of C5a and formation of
C5b-9 (also known as the membrane attack complex, or MAC), and independently also inhibits leukotriene B4, or LTB4, activity,
both elements that are co-located as part of the immune/inflammatory response. Nomacopan (Coversin) is a recombinant small protein
(16,740 Da) derived from a protein originally discovered in the saliva of the Ornithodoros moubata tick, where it modulates the
host immune system to allow the parasite to feed without alerting the host to its presence or provoking an immune response.
Nomacopan (Coversin) has received orphan drug
status from the U.S. Food and Drug Administration, or the FDA, and the European Medicines Agency, or the EMA, for paroxysmal nocturnal
haemoglobinuria, or PNH, and Guillain Barr Syndrome, or GBS. Orphan drug designation provides us with certain benefits
and incentives, including a period of marketing exclusivity if regulatory approval of the drug is ultimately received for the designated
indication. The receipt of orphan drug designation status does not change the regulatory requirements or process for obtaining
marketing approval and the designation does not mean that marketing approval will be received. We intend to apply in the future
for orphan drug designation in additional indications we deem appropriate.
Last updated: Jun 6, 2019