Current Report Filing (8-k)
May 13 2021 - 8:35AM
Edgar (US Regulatory)
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): May 12, 2021
REGEN BIOPHARMA, INC.
(Exact name of small business issuer
as specified in its charter)
Nevada
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45-5192997
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(State or other jurisdiction of incorporation or organization)
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(I.R.S. Employer Identification No.)
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Commission File No. 333-191725
711 S. Carson Street, Suite 4, Carson
City, Nevada, 89791
(Address of Principal Executive Offices)
(619) 722 5505
(Issuer’s telephone number)
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))
Item 8.01 Other Events.
On May 12, 2021 Regen
Biopharma, Inc. (the “Company”) executed a consulting agreement with Biotech Research Group Corporation (the “Consultant”),
an FDA Specialist Group and Global Regulatory and Scientific Experts, for the purpose of review and guidance with regard to the
planned reinstatement of the Company’s inactive Investigational New Drug applications (INDs) #15376 and #16200 filed with
the United States Food and Drug Administration (“FDA”). The securing of the services to be provided to the Company
pursuant to this consulting agreement marks the first step taken by the Company with regard to activating the Company’s currently
inactive applications to initiate clinical trials.
In December 2015 Company
was granted permission by the FDA allowing for initiation of clinical trials of the Company’s HemaXellerate therapy under
its IND #15376. HemaXellerate is a personalized immune-modulatory cell therapy that has demonstrated benefit in animal models of
aplastic anemia.
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 hereunto duly authorized.
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REGEN BIOPHARMA, INC.
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Dated: May 13, 2021
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By: /s/ David Koos
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David Koos
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Chief Executive Officer
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