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UNITED
STATES
SECURITIES
AND EXCHANGE COMMISSION
Washington,
D.C. 20549
FORM
8-K
CURRENT
REPORT
Pursuant
to Section 13 or 15(d) of the Securities Exchange Act of 1934
Date
of Report (date of earliest event reported): August 9, 2024
Serina
Therapeutics, Inc.
(Exact
name of registrant as specified in its charter)
Delaware |
|
1-38519 |
|
82-1436829 |
(State
or other jurisdiction |
|
(Commission |
|
(IRS
Employer |
of
incorporation) |
|
File
Number) |
|
Identification
No.) |
601
Genome Way, Suite 2001
Huntsville,
Alabama 35806
(Address
of principal executive offices)
(256)
327-9630
(Registrant’s
telephone number, including area code)
Not
applicable
(Former
name or former address, if changed since last report)
Check
the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under
any of the following provisions:
☐ |
Written
communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425) |
|
|
☐ |
Soliciting
material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12) |
|
|
☐ |
Pre-commencement
communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b)) |
|
|
☐ |
Pre-commencement
communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c)) |
Securities
registered pursuant to Section 12(b) of the Act:
Title
of each class |
|
Trading
Symbol |
|
Name
of exchange on which registered |
Common
Stock, par value $0.0001 per share |
|
SER |
|
NYSE
American |
Indicate
by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405
of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).
Emerging
growth company ☒
If
an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying
with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act.
Any
statements that are not historical fact (including, but not limited to statements that contain words such as “may,” “will,”
“believes,” “plans,” “intends,” “anticipates,” “expects,” “estimates”)
should also be considered to be forward-looking statements. Additional factors that could cause actual results to differ materially from
the results anticipated in these forward-looking statements are contained in Serina’s periodic reports filed with the Securities
and Exchange Commission (the “SEC”) under the heading “Risk Factors” and other filings that Serina may make with
the SEC. Undue reliance should not be placed on these forward-looking statements which speak only as of the date they are made, and the
facts and assumptions underlying these statements may change. Except as required by law, Serina disclaims any intent or obligation to
update these forward-looking statements.
References
in this Report to “Serina,” “the Company,” “we” or “us” refer to Serina Therapeutics,
Inc.
Item
2.02 Results of Operations and Financial Condition
On
August 9, 2024, the Company issued a press release announcing its financial results for the quarter and six months ended June 30, 2024.
A copy of the press release is furnished as Exhibit 99.1 hereto.
The
information in this Item 2.02 and in the press release furnished as Exhibit 99.1 to this current report shall not be deemed to be “filed”
for purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), and is not to be incorporated
by reference into any filing of the registrant under the Securities Act of 1933, as amended, or the Exchange Act, whether made before
or after the date hereof, regardless of any general incorporation language in any such filing, except as shall be expressly set forth
by specific reference in such a filing.
Item
9.01 - Financial Statements and Exhibits.
SIGNATURES
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 hereunto duly authorized.
|
SERINA
THERAPEUTICS, INC. |
|
|
|
Date:
August 9, 2024 |
By: |
/s/
Andrea Park |
|
|
Interim
Chief Financial Officer |
Exhibit
99.1
Serina
Therapeutics Reports Second Quarter 2024 Financial Results and Provides Business Highlights
HUNTSVILLE,
August 9, 2024 (GLOBE NEWSWIRE) — Serina Therapeutics (“Serina”) (NYSE American: SER), a clinical-stage
biotechnology company developing its proprietary POZ Platform™ drug delivery technology, today reported financial results for the
quarter ended June 30, 2024 and provided business highlights.
Recent
Highlights
|
● |
Partnership
with Enable Injections. The Company will develop and commercialize SER-252 (POZ-apomorphine) in combination with enFuseTM
for the treatment of Parkinson’s disease. The enFuseTM wearable technology from Enable is designed to overcome
both IV infusion and other subcutaneous administration method shortcomings through fast, simple, and convenient delivery, benefiting
patients, providers, as well as payers, with the ability for at home self-administration. The Company anticipates submission of an
Investigational New Drug (IND) application to the U.S. Food and Drug Administration with plans to initiate a Phase 1 clinical trial
in advanced Parkinson’s disease patients in 2025. |
|
|
|
|
● |
Presentation
of POZ-lipid immunogenicity data. The Company presented novel data on Serina’s innovative POZ-lipid, a proprietary technology
that aims to significantly advance the safety and efficacy of mRNA-LNP formulations. These data show that POZ-lipid does not induce
an IgM or IgG antibody response, even with repeated dosing in in vivo models. This finding is crucial because the PEG-lipids currently
used in mRNA vaccines can elicit an anti-PEG antibody response. This response is associated with serious adverse events, including
anaphylaxis, which can pose a life-threatening risk to patients. Serina’s POZ-lipid technology can potentially mitigate these
adverse effects, thereby enhancing the safety and efficacy profile of mRNA-LNP medicines. |
|
|
|
|
● |
Appointment
of Dr. Srini Tenjarla as Senior Vice President of CMC & Formulation. Dr. Tenjarla joins Serina Therapeutics from Takeda Pharmaceuticals,
where he served as Vice President and Head of Drug Product Development and Process Chemistry Development/Outsourcing in Pharmaceutical
Sciences. Prior to his tenure at Takeda, Dr. Tenjarla held several leadership roles at Shire Pharmaceuticals, culminating in his
position as Vice President of Pharmaceutical Sciences. Dr. Tenjarla has a proven track record in advancing programs through clinical
phases to NDA/BLA submission and approval. |
Liquidity
and Capital Resources
On
May 8, 2024, the repayment date of the Company’s borrowings under the Juvenescence Secured Note was extended from May 9,
2024 to December 31, 2024 and the line of credit increased by an additional $525,000 which we received entirely on May 9, 2024.
Balance
Sheet Information
Cash,
cash equivalents, and restricted cash totaled $6.1 million as of June 30, 2024. As of June 30, 2024, the Company owed Juvenescence Limited
$11.2 million in principal and origination fees on account of loans extended to the Company.
Second
Quarter Operating Results
Revenues:
Revenues comprised entirely of grant revenues from the National Institutes of Health in the amount of $51,000 and $7,000 for the
second quarter of 2024 and in the same period in 2023, respectively.
Operating
expenses: Operating expenses for the three months ended June 30, 2024 were $3.9 million, as compared with $1 million for the same
period in 2023.
Research
and development expenses for the three months ended June 30, 2024 increased by approximately $1.1 million to $1.6 million from $0.5 million
during the same period in 2023. The net increase was primarily attributable to a non-recurring $0.3 million severance expense,
increases of $0.4 million in salaries and payroll related expenses and consulting services allocable to research and development expenses,
$0.3 million in patent related professional fees primarily for the maintenance of certain patent and other intellectual property and
biological material assets included in Legacy Assets, and $0.1 million in laboratory supplies and depreciation expenses allocable to
research and development expenses.
General
and administrative expenses for the three months ended June 30, 2024 increased by $1.8 million to $2.3 million as compared to
$0.5 million during the same period in 2023. The net increase is attributable to increases of $0.6 million in professional legal and
accounting services incurred largely in connection with the Merger which consummated on March 26, 2024, $0.5 million in director compensation
and consulting services and noncash stock-based compensation for options granted to directors and consultants allocable to general and
administrative expenses, $0.2 million in insurance expenses, $0.2 million in market research and Company website development related
expenses, $0.1 million in salaries and payroll related expenses allocable to general and administrative expenses, $0.1 million in recruiting
and hiring expenses, $0.1 million in rent and facilities maintenance related expenses, and $0.1 million in investor and public relations
related expenses. These increases were offset to some extent by a $0.1 million decrease in miscellaneous expenses.
Other
income, net: Net other income for the three months ended June 30, 2024 is primarily comprised of $9.3 million change in fair value
of derivative warrant liabilities offset to some extent by $0.3 million amortization of deferred debt issuance costs and other debt related
expenses.
Net
income: The net income attributable to Serina for the three months ended June 30, 2024 was $5.2 million, or $0.61 per share (basic)
and $0.51 per share (diluted) compared to net income of $0.8 million, or $0.37 per share (basic) and $0.11 per share (diluted), for 2023.
Net loss for the three months ended June 30, 2024 as compared to net income in 2023 is partially attributable to the ramp up of operating
activities following the consummation of the Merger on March 26, 2024 offset by the net change in fair value of derivative warrant liabilities
and convertible promissory notes.
Going
Concern Considerations
As
required under Accounting Standards Update 2014-15, Presentation of Financial Statements-Going Concern (ASC 205-40), the Company
evaluates whether conditions and/or events raise substantial doubt about its ability to meet its future financial obligations as they
become due within one year after the date its financial statements are issued. Based on the Company’s most recent projected cash
flows, the Company believes that its cash and cash equivalents of $6.1 million as of June 30, 2024 along with the approximately $10 million
of cash proceeds expected to be received from Juvenescence through the exercise of Juvenescence’s remaining Post-Merger Warrants
as provided in a “Side Letter” would not be sufficient to satisfy the Company’s anticipated operating and other funding
requirements for the twelve months following the filing of the Company’s Quarterly Report on Form 10-Q for the three and six months
ended June 30, 2024. These factors raise substantial doubt regarding the ability of the Company to continue as a going concern.
About
SER-252 (POZ-apomorphine)
SER
252 is an investigational apomorphine therapy developed with Serina’s POZ platform and designed to provide continuous dopaminergic
stimulation (CDS). CDS has been shown to reduce the severity of levodopa-related motor complications (dyskinesia) in Parkinson’s
disease. Preclinical studies support the potential of SER 252 to provide CDS without skin reactions. Serina plans to advance SER 252
to clinical testing in 2025.
About
the POZ Platform™
Serina’s
proprietary POZ technology is based on a synthetic, water soluble, low viscosity polymer called poly(2-oxazoline). Serina’s POZ
technology is engineered to provide greater control in drug loading and more precision in the rate of release of attached drugs delivered
via subcutaneous injection. The therapeutic agents in Serina’s product candidates are typically well-understood and marketed drugs
that are effective but are limited by pharmacokinetic profiles that can include toxicity, side effects and short half-life. Serina believes
that by using POZ technology, drugs with narrow therapeutic windows can be designed to maintain more desirable and stable levels in the
blood.
Serina’s
POZ platform delivery technology has potential for use across a broad range of payloads and indications. Serina intends to advance additional
applications of the POZ platform via out-licensing, co-development, or other partnership arrangements, including the non-exclusive license
agreement with Pfizer, Inc. to use Serina’s POZ polymer technology for use in lipid nanoparticle drug (LNP) delivery formulations.
About
Serina Therapeutics
Serina
is a clinical-stage biotechnology company developing a pipeline of wholly owned drug product candidates to treat neurological diseases
and pain. Serina’s POZ PlatformTM delivery technology is engineered to provide greater control in drug loading and more
precision in the rate of release of attached drugs, enabling the potential of challenging small molecules, while addressing the limitations
of PEG (polyethylene glycol) and other biocompatible polymers. In addition, our POZ PlatformTM partners are at the forefront
in advancing lipid nanoparticle (LNP) delivery technology to develop novel RNA therapeutics. Serina is headquartered in Huntsville, Alabama
on the campus of the HudsonAlpha Institute of Biotechnology.
For
more information, please visit https://serinatherapeutics.com.
Cautionary
Statement Regarding Forward-Looking Statement
This
release contains forward-looking statements within the meaning of federal securities laws. These statements are based on management’s
current expectations, plans, beliefs or forecasts for the future, and are subject to uncertainty and changes in circumstances. Any express
or implied statements in this press release that are not statements of historical fact, including statements about the potential of Serina’s
POZ polymer technology, are forward-looking statements that involve substantial risks and uncertainties that could cause actual results
to differ materially from those expressed or implied by such statements. Risks and uncertainties include, among other things, the uncertainties
inherent in research and development, including the ability to meet anticipated clinical endpoints, commencement and/or completion dates
for clinical trials, regulatory submission dates, regulatory approval dates and/or launch dates, as well as the possibility of unfavorable
new clinical data and further analyses of existing clinical data; the risk that clinical trial data are subject to differing interpretations
and assessments by regulatory authorities; whether regulatory authorities will be satisfied with the design of and results from our clinical
studies; whether and when any applications may be filed for any drug or vaccine candidates in any jurisdictions; whether and when regulatory
authorities may approve any potential applications that may be filed for any drug or vaccine candidates in any jurisdictions, which will
depend on a myriad of factors, including making a determination as to whether the product’s benefits outweigh its known risks and
determination of the product’s efficacy and, if approved, whether any such drug or vaccine candidates will be commercially successful;
decisions by regulatory authorities impacting labeling, manufacturing processes, safety and/or other matters that could affect the availability
or commercial potential of any drug or vaccine candidates; and competitive developments. These risks as well as other risks are more fully discussed in the company’s
Annual Report on Form 10-K for the year ended December 31, 2023, the company’s Current Report on Form 8-K that was filed with the
SEC on April 1, 2024, and the company’s other periodic reports and documents filed from time to time with the SEC.
The
Information contained in this release Is as of the date hereof, and Serina assumes no obligation to update forward-looking statements
contained in this release as the result of new information or future events or developments.
For
inquiries, please contact:
Investor.relations@serinatherapeutics.com
(256)
327-9630
SERINA
THERAPEUTICS, INC. AND SUBSIDIARIES
CONDENSED
CONSOLIDATED BALANCE SHEETS
(in
thousands, except par value amounts)
| |
June 30, 2024 | | |
December 31, 2023 | |
| |
| (unaudited) | | |
| | |
ASSETS | |
| | | |
| | |
Current assets: | |
| | | |
| | |
Cash and cash equivalents | |
$ | 6,064 | | |
$ | 7,619 | |
Grant receivable | |
| 51 | | |
| - | |
Prepaid expenses and other current assets | |
| 2,802 | | |
| - | |
Total current assets | |
| 8,917 | | |
| 7,619 | |
| |
| | | |
| | |
Restricted cash | |
| 50 | | |
| - | |
Property and equipment, net | |
| 540 | | |
| 573 | |
Right of use assets - operating leases | |
| 562 | | |
| 666 | |
Right of use assets - finance leases | |
| 98 | | |
| 110 | |
Intangible assets, net | |
| 541 | | |
| - | |
TOTAL ASSETS | |
$ | 10,708 | | |
$ | 8,968 | |
| |
| | | |
| | |
LIABILITIES, REDEEMABLE CONVERTIBLE PREFERRED STOCK, AND STOCKHOLDERS’ DEFICIT | |
| | | |
| | |
Current liabilities: | |
| | | |
| | |
Accounts payable and accrued liabilities | |
$ | 1,972 | | |
$ | 1,163 | |
Loans due to Juvenescence, net of debt issuance costs | |
| 10,445 | | |
| - | |
Current portion of operating lease liabilities | |
| 200 | | |
| 214 | |
Current portion of finance lease liabilities | |
| 11 | | |
| 36 | |
Other current liabilities | |
| 5 | | |
| - | |
Total current liabilities | |
| 12,633 | | |
| 1,413 | |
| |
| | | |
| | |
Warrant liability | |
| 13,413 | | |
| - | |
Loans due to Juvenescence | |
| 693 | | |
| - | |
Convertible promissory notes, at fair value | |
| - | | |
| 2,983 | |
Operating lease liabilities, net of current portion | |
| 362 | | |
| 461 | |
Finance lease liabilities, net of current portion | |
| - | | |
| 1 | |
TOTAL LIABILITIES | |
| 27,101 | | |
| 4,858 | |
| |
| | | |
| | |
Commitments and contingencies | |
| | | |
| | |
| |
| | | |
| | |
Redeemable Convertible Preferred Stock: | |
| | | |
| | |
Redeemable convertible preferred stock, $0.01 par value; 10,000 authorized; nil and 3,438 issued and outstanding at June 30, 2024 and December 31, 2023, respectively | |
| - | | |
| 36,404 | |
Stockholders’ deficit: | |
| | | |
| | |
Preferred stock, $0.0001 par value, 5,000 shares authorized; none issued and outstanding | |
| - | | |
| - | |
Common stock, $0.0001 par value, 40,000 shares authorized; and 8,792 and 2,410 shares issued and outstanding | |
| 1 | | |
| 25 | |
Additional paid-in capital | |
| 6,821 | | |
| 858 | |
Accumulated deficit | |
| (23,185 | ) | |
| (33,177 | ) |
Total Serina Therapeutics, Inc. stockholders’ deficit | |
| (16,363 | ) | |
| (32,294 | ) |
Noncontrolling interest | |
| (30 | ) | |
| - | |
Total stockholders’ deficit | |
| (16,393 | ) | |
| (32,294 | ) |
TOTAL LIABILITIES, REDEEMABLE CONVERTIBLE PREFERRED STOCK, AND STOCKHOLDERS’ DEFICIT | |
$ | 10,708 | | |
$ | 8,968 | |
SERINA
THERAPEUTICS, INC. AND SUBSIDIARIES
CONDENSED
CONSOLIDATED STATEMENTS OF OPERATIONS
(in
thousands, except per share data)
(unaudited)
| |
Three Months Ended June 30, | | |
Six Months Ended June 30, | |
| |
2024 | | |
2023 | | |
2024 | | |
2023 | |
REVENUES | |
| | | |
| | | |
| | | |
| | |
Grant revenues | |
$ | 51 | | |
$ | 7 | | |
$ | 56 | | |
$ | 37 | |
Total revenues | |
| 51 | | |
| 7 | | |
| 56 | | |
| 37 | |
| |
| | | |
| | | |
| | | |
| | |
OPERATING EXPENSES | |
| | | |
| | | |
| | | |
| | |
Research and development | |
| 1,594 | | |
| 479 | | |
| 2,700 | | |
| 878 | |
General and administrative | |
| 2,323 | | |
| 473 | | |
| 3,543 | | |
| 1,066 | |
Total operating expenses | |
| 3,917 | | |
| 952 | | |
| 6,243 | | |
| 1,944 | |
| |
| | | |
| | | |
| | | |
| | |
Loss from operations | |
| (3,866 | ) | |
| (945 | ) | |
| (6,187 | ) | |
| (1,907 | ) |
| |
| | | |
| | | |
| | | |
| | |
OTHER INCOME (EXPENSE), NET | |
| | | |
| | | |
| | | |
| | |
Interest expense, net | |
| (242 | ) | |
| (108 | ) | |
| (341 | ) | |
| (194 | ) |
Fair value inception adjustment on convertible promissory note | |
| - | | |
| - | | |
| - | | |
| 2,240 | |
Change in fair value of convertible promissory notes | |
| - | | |
| 1,570 | | |
| (7,017 | ) | |
| 1,864 | |
Change in fair value of warrants | |
| 9,294 | | |
| 291 | | |
| 3,716 | | |
| 463 | |
Other expense, net | |
| (9 | ) | |
| - | | |
| (9 | ) | |
| - | |
Total other income (expense), net | |
| 9,043 | | |
| 1,753 | | |
| (3,651 | ) | |
| 4,373 | |
| |
| | | |
| | | |
| | | |
| | |
NET INCOME (LOSS) | |
| 5,177 | | |
| 808 | | |
| (9,838 | ) | |
| 2,466 | |
Net loss attributable to noncontrolling interest | |
| 27 | | |
| - | | |
| 27 | | |
| - | |
| |
| | | |
| | | |
| | | |
| | |
NET INCOME (LOSS) ATTRIBUTABLE TO SERINA | |
$ | 5,204 | | |
$ | 808 | | |
$ | (9,811 | ) | |
$ | 2,466 | |
| |
| | | |
| | | |
| | | |
| | |
NET EARNINGS (LOSS) PER COMMON SHARE: | |
| | | |
| | | |
| | | |
| | |
BASIC | |
$ | 0.61 | | |
$ | 0.37 | | |
$ | (1.74 | ) | |
$ | 1.14 | |
DILUTED | |
$ | 0.51 | | |
$ | 0.11 | | |
$ | (1.74 | ) | |
$ | 0.34 | |
| |
| | | |
| | | |
| | | |
| | |
WEIGHTED AVERAGE NUMBER OF COMMON SHARES OUTSTANDING: | |
| | | |
| | | |
| | | |
| | |
BASIC | |
| 8,514 | | |
| 2,172 | | |
| 5,652 | | |
| 2,170 | |
DILUTED | |
| 10,157 | | |
| 7,434 | | |
| 5,652 | | |
| 7,427 | |
SERINA
THERAPEUTICS, INC. AND SUBSIDIARIES
CONDENSED
CONSOLIDATED STATEMENTS OF CASH FLOWS
(in
thousands)
(unaudited)
| |
Six Months Ended June 30, | |
| |
2024 | | |
2023 | |
OPERATING ACTIVITIES: | |
| | | |
| | |
Net income (loss) attributable to Serina | |
$ | (9,811 | ) | |
$ | 2,466 | |
Net income (loss) attributable to noncontrolling interest | |
| (27 | ) | |
| - | |
Adjustments to reconcile net income (loss) attributable to Serina to net cash used in operating activities: | |
| | | |
| | |
Depreciation and amortization | |
| 82 | | |
| 30 | |
Non-cash lease expense | |
| 116 | | |
| 90 | |
Amortization of debt issuance costs | |
| 329 | | |
| - | |
Stock-based compensation | |
| 511 | | |
| 25 | |
Fair value inception adjustment on convertible promissory note | |
| - | | |
| (2,240 | ) |
Change in fair value of convertible promissory notes | |
| 7,017 | | |
| (1,864 | ) |
Change in fair value of warrants | |
| (3,716 | ) | |
| (463 | ) |
Changes in operating assets and liabilities: | |
| | | |
| | |
Grant receivable | |
| 15 | | |
| - | |
Prepaid expenses and other current assets | |
| (2,694 | ) | |
| 1 | |
Accounts payable and accrued liabilities | |
| (1,398 | ) | |
| 185 | |
Accrued interest on convertible promissory notes | |
| 163 | | |
| 282 | |
Operating lease liabilities | |
| (112 | ) | |
| (85 | ) |
Related party payables | |
| (66 | ) | |
| - | |
Other current liabilities | |
| 5 | | |
| - | |
Net cash used in operating activities | |
| (9,586 | ) | |
| (1,573 | ) |
| |
| | | |
| | |
INVESTING ACTIVITIES: | |
| | | |
| | |
Purchase of equipment | |
| (14 | ) | |
| (315 | ) |
Net cash used in investing activities | |
| (14 | ) | |
| (315 | ) |
| |
| | | |
| | |
FINANCING ACTIVITIES: | |
| | | |
| | |
Drawdown on loan facilities from Juvenescence | |
| 2,925 | | |
| - | |
Cash and restricted cash acquired in connection with the Merger | |
| 337 | | |
| - | |
Proceeds from the exercise of stock options | |
| 4 | | |
| 1 | |
Proceeds from the exercise of Post-Merger Warrants by Juvenescence | |
| 4,988 | | |
| - | |
Proceeds from the issuance of convertible promissory notes | |
| - | | |
| 10,100 | |
Principal repayment on loan facilities to Juvenescence | |
| (133 | ) | |
| - | |
Principal repayments on finance lease liabilities | |
| (26 | ) | |
| (23 | ) |
Net cash provided by financing activities | |
| 8,095 | | |
| 10,078 | |
| |
| | | |
| | |
NET CHANGE IN CASH, CASH EQUIVALENTS AND RESTRICTED CASH | |
| (1,505 | ) | |
| 8,190 | |
| |
| | | |
| | |
CASH, CASH EQUIVALENTS AND RESTRICTED CASH: | |
| | | |
| | |
At beginning of the period | |
| 7,619 | | |
| 532 | |
At end of the period | |
$ | 6,114 | | |
$ | 8,722 | |
v3.24.2.u1
Cover
|
Aug. 09, 2024 |
Cover [Abstract] |
|
Document Type |
8-K
|
Amendment Flag |
false
|
Document Period End Date |
Aug. 09, 2024
|
Entity File Number |
1-38519
|
Entity Registrant Name |
Serina
Therapeutics, Inc.
|
Entity Central Index Key |
0001708599
|
Entity Tax Identification Number |
82-1436829
|
Entity Incorporation, State or Country Code |
DE
|
Entity Address, Address Line One |
601
Genome Way
|
Entity Address, Address Line Two |
Suite 2001
|
Entity Address, City or Town |
Huntsville
|
Entity Address, State or Province |
AL
|
Entity Address, Postal Zip Code |
35806
|
City Area Code |
(256)
|
Local Phone Number |
327-9630
|
Written Communications |
false
|
Soliciting Material |
false
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Serina Therapeutics (AMEX:SER)
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Serina Therapeutics (AMEX:SER)
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Von Jan 2024 bis Jan 2025