Report of Foreign Issuer Pursuant to Rule 13a-16 or 15d-16 (6-k)
25 October 2022 - 07:31AM
Edgar (US Regulatory)
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM 6-K
REPORT OF FOREIGN PRIVATE ISSUER PURSUANT TO RULE 13a-16
OR 15d-16 UNDER THE SECURITIES EXCHANGE ACT OF 1934
For the month of October 2022
Commission File Number: 001-36582
Altamira Therapeutics Ltd.
(Exact name of registrant as specified in its charter)
Clarendon House,
2 Church Street
Hamilton HM11, Bermuda
(Address of principal executive office)
Indicate by check mark whether the registrant files or will file
annual reports under cover of Form 20-F or Form 40-F:
Form 20-F ☒ Form
40-F ☐
Indicate by check mark if the registrant is submitting the Form 6-K
in paper as permitted by Regulation S-T Rule 101(b)(1):
Yes ☐ No
☒
Indicate by check mark if the registrant is submitting the Form 6-K
in paper as permitted by Regulation S-T Rule 101(b)(7):
Yes ☐ No
☒
On October 19, 2022, Altamira Therapeutics Ltd., an exempted
company limited by shares incorporated in Bermuda (the “Company”),
entered into a share purchase agreement (the “SPA”) with a European
family office (the “Buyer”), pursuant to which the Buyer agreed to
acquire 90% of the share capital of the Company’s subsidiary
Zilentin Ltd., Zug (Switzerland) (“Zilentin”) for immediate cash
consideration of $1 million. Zilentin has been active in the
research for novel, second generation tinnitus treatments in
collaboration with leading academic partners (project AM-102). At
the closing of such acquisition (expected on or about October 28,
2022) (the “Initial Closing”), Zilentin has agreed to purchase from
the Company, for immediate cash consideration of another $1
million, an option (the “Option”), pursuant to an option agreement
dated October 19, 2022 (the “Option Agreement”) that entitles
Zilentin to acquire (such acquisition, “Transaction 2”) all (and
not part) of the Company’s remaining legacy assets in inner ear
therapeutics, including AM-101 (tinnitus), AM-111 (hearing loss)
and AM-125 (vertigo), for an upfront payment of $25 million in cash
upon exercise.
The Option may be exercised for 30 days following the date of the
Option Agreement. Beyond the 30 days, Zilentin will have a right of
first refusal to acquire the subject assets until December 31,
2022, with the $25 million option-exercise payment increasing by $1
million every 30-day increment following the initial date of the
Option Agreement.
After an exercise of the Option by Zilentin (or purchase of the
assets otherwise before December 31, 2022), if any, the Company
will be entitled to receive milestone payments of up to $55 million
in the aggregate as well as royalties. The milestones relate to
certain development or regulatory milestones, and are as
follows:
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the acceptance of an
investigational new drug application by the U.S. Federal Drug
Administration for AM-125 ($5 million); |
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a successful Phase 3 study for
AM-125 ($10 million); |
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the regulatory approval for AM-125
in vertigo ($10 million); |
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the regulatory approval of AM-101
in acute inner ear tinnitus ($10 million); |
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the regulatory approval of AM-111
in acute inner ear hearing loss ($10 million); and |
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the grant of a license for the
Company’s RNA delivery technology to Zilentin for certain targets
in inner ear disorders, on or before December 31, 2024 ($10 million
upfront plus a mid-single digit percentage in royalties on future
revenues generated from the sale of drug products making use of the
technology). |
Assuming the Option is exercised (or Zilentin otherwise purchases
the assets before December 31, 2022), the Option Agreement provides
that prior to the closing of Transaction 2, the Company’s CEO,
Thomas Meyer, will become the CEO of Zilentin within six months
after such closing, while also retaining a reasonable amount of
time to continue serving as the principal executive of the Company
together with the current RNA business leadership team.
The Option Agreement may be terminated by either party if the
closing of Transaction 2 has not occurred on or before December 31,
2022.
There is no assurance that Zilentin will exercise the Option or
otherwise purchase the assets subject to the Option Agreement. The
closing of Transaction 2 is subject to the parties’ finalizing of
the definitive documents related thereto, and the grant of the
license to Zilentin for RNA delivery technology for inner ear
disorders is subject to the negotiation and agreement between the
parties on such license.
The SPA and the Option Agreement also contain customary
representations, warranties and covenants by the parties, as well
as customary provisions relating to indemnification,
confidentiality and other matters.
The foregoing description of the terms of the SPA and the Option
Agreement is qualified in its entirety by reference to the full
text of such documents, which are furnished as Exhibits 99.1 and
99.2, respectively, to this Report on Form 6-K, and incorporated by
reference herein.
INCORPORATION BY REFERENCE
This Report on Form 6-K shall be deemed to be incorporated by
reference into the registration statements on Form F-3
(Registration Numbers
333-228121,
333-249347,
333-261127 and
333-264298) and Form S-8 (Registration Numbers
333-232735 and
333-252141) of Altamira Therapeutics Ltd. (formerly Auris
Medical Holding Ltd.) and to be a part thereof from the date on
which this report is filed, to the extent not superseded by
documents or reports subsequently filed or furnished.
EXHIBIT INDEX
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* |
Certain identified information has
been excluded from this Exhibit because it is not material and is
the type that the Company treats as private or confidential. The
omissions have been indicated by “[**]”. |
SIGNATURE
Pursuant to the requirements of the Securities Exchange Act of
1934, the registrant has duly caused this report to be signed on
its behalf by the undersigned, thereunto duly authorized.
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Altamira
Therapeutics Ltd. |
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By: |
/s/ Marcel Gremaud |
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Name: |
Marcel Gremaud |
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Title: |
Chief Financial
Officer |
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Date: October 24,
2022 |
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