0001140361-21-028462.txt : 20210816 0001140361-21-028462.hdr.sgml : 20210816 20210816162714 ACCESSION NUMBER: 0001140361-21-028462 CONFORMED SUBMISSION TYPE: 8-K PUBLIC DOCUMENT COUNT: 14 CONFORMED PERIOD OF REPORT: 20210816 ITEM INFORMATION: Results of Operations and Financial Condition ITEM INFORMATION: Financial Statements and Exhibits FILED AS OF DATE: 20210816 DATE AS OF CHANGE: 20210816 FILER: COMPANY DATA: COMPANY CONFORMED NAME: Kinnate Biopharma Inc. CENTRAL INDEX KEY: 0001797768 STANDARD INDUSTRIAL CLASSIFICATION: PHARMACEUTICAL PREPARATIONS [2834] IRS NUMBER: 824566526 STATE OF INCORPORATION: DE FISCAL YEAR END: 1231 FILING VALUES: FORM TYPE: 8-K SEC ACT: 1934 Act SEC FILE NUMBER: 001-39743 FILM NUMBER: 211178745 BUSINESS ADDRESS: STREET 1: 11975 EL CAMINO REAL, STE 101 CITY: SAN DIEGO STATE: CA ZIP: 92130 BUSINESS PHONE: 8582994699 MAIL ADDRESS: STREET 1: 11975 EL CAMINO REAL, STE 101 CITY: SAN DIEGO STATE: CA ZIP: 92130 8-K 1 brhc10028061_8k.htm 8-K
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 16, 2021


KINNATE BIOPHARMA INC.
(Exact name of registrant as specified in its charter)


Delaware
 
001-39743
 
82-4566526
(State or other jurisdiction of incorporation)
 
(Commission File Number)
 
(IRS Employer Identification No.)

3611 Valley Centre Drive, Suite 175
San Diego, CA 92130
(Address of principal executive offices, including zip code)

(858) 299-4699
 (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 (see General Instruction A.2. below):

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(s)
Name of each exchange on which
registered
Common Stock, $0.0001 par value per share
KNTE
The NASDAQ Global Select Market
 
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.



Item 2.02
Results of Operations and Financial Condition.
 
On August 16, 2021, Kinnate Biopharma Inc. issued a press release announcing its financial results for the quarter ended June 30, 2021.  A copy of the press release is attached hereto as Exhibit 99.1 and is incorporated herein by reference.
 
All of the information furnished in this Item 2.02 and Item 9.01 (including Exhibit 99.1) shall not be deemed to be “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), or otherwise subject to the liabilities of that section, nor shall it be deemed incorporated by reference into any filing under the Securities Act of 1933, as amended, or the Exchange Act, except as shall be expressly set forth by specific reference in such a filing.
 
Item 9.01
Financial Statements and Exhibits.
 
(d) Exhibits

Exhibit No.
 
Description
   
 
Press Release dated August 16, 2021


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.



KINNATE BIOPHARMA INC.


Date: August 16, 2021
By:
/s/ Nima Farzan


Nima Farzan


President and Chief Executive Officer



EX-99.1 2 brhc10028061_ex99-1.htm EXHIBIT 99.1

Exhibit 99.1


Kinnate Biopharma Inc. Reports Second Quarter 2021 Financial Results

Announced first patient dosed in Phase 1 trial
evaluating KIN-2787 in patients with BRAF mutation-positive solid tumors

Strengthened management team and Board of Directors with key appointments

Ended the quarter with cash, cash equivalents and investments of $365.1 million, exclusive of $35.0 million in its China joint venture

SAN FRANCISCO and SAN DIEGO, Calif. – August 16, 2021 – Kinnate Biopharma Inc. (Nasdaq: KNTE) (“Kinnate”), a biopharmaceutical company focused on the discovery and development of small molecule kinase inhibitors for difficult-to-treat, genomically defined cancers, today announced financial results for the quarter ended June 30, 2021. The company also announced that the first patient has commenced treatment in its Phase 1 KN-8701 clinical trial evaluating its lead RAF product candidate, KIN-2787, a pan-RAF inhibitor being developed for the treatment of patients with lung cancer, melanoma and other solid tumors.

“2021 continues to be a year of progress for Kinnate. Initiating our first in-human trial for KIN-2787 and dosing our first patient were important steps forward toward expanding options for cancer patients who are not benefiting from currently approved RAF inhibitors," said Nima Farzan, Chief Executive Officer of Kinnate. "As we enter the second half of the year, our expanding team of clinical and business leaders are well positioned to drive further progress in our KIN-2787 program and advance our pipeline of targeted precision oncology therapies, including our lead FGFR inhibitor candidate for which we anticipate filing an IND in the first half of 2022.”

The KN-8701 trial is a multi-center, open-label, two-part study of approximately 115 patients to evaluate the safety, tolerability, pharmacokinetics (PK), and preliminary efficacy of KIN-2787 in adults with Class I, Class II, or Class III BRAF-mutated advanced or metastatic solid tumors.

"Successfully targeting patients with Class II and Class III BRAF mutations remains a substantial unmet need in cancer care. KIN-2787 brings a unique approach to potentially address the shortcomings of existing therapies by inhibiting dimer signaling in specific patient populations with BRAF mutations while also minimizing MAPK paradoxical activation," said Meredith McKean, MD, MPH, Associate Director, Melanoma and Skin Cancer Research Program, Sarah Cannon Research Institute at Tennessee Oncology. "We are proud to be the first site to treat a patient with KIN-2787 and look forward to working with Kinnate to continue enrollment in this important Phase 1 trial.”

Other Recent Business Highlights and Corporate Update:


In May 2021, we closed a $35 million Series A preferred stock financing of a China joint venture (“China JV”), of which Kinnate is the majority shareholder. Established with OrbiMed Asia Partners, OrbiMed Private Investments and Foresite Capital, the China JV will be headquartered in Shanghai and the financing will enable the potential development and commercialization by the China JV of certain Kinnate targeted oncology product candidates across Greater China (PRC, Hong Kong, Taiwan, and Macau).

We appointed Neha Krishnamohan as our Chief Financial Officer and Executive Vice President, Corporate Development, and we continued to expand our leadership team, including with the appointment of Ken Kobayashi, M.D., our Senior Vice President, Clinical Development.

Helen Sabzevari, Ph.D. was appointed to our Board of Directors, and Stephen Kaldor, Ph.D., one of our founders, was not nominated for re-election to our Board of Directors when his term expired at our 2021 annual meeting of shareholders.



We expanded our organization to 52 full-time employees at June 30, 2021, of which 39 were engaged in research and development activities.

During a virtual poster session at the 57th Annual Meeting of the American Society of Clinical Oncology (ASCO), we presented results from preclinical studies evaluating the efficacy and tolerability of KIN-2787, in vitro and in vivo in BRAF mutation-driven human cancer models.

Second Quarter 2021 Financial Results


Second quarter net loss for 2021 was $21.4 million, compared to $7.6 million for the same period in 2020.

Second quarter research and development expenses for 2021 were $16.2 million, compared to $5.6 million for the same period in 2020.

Second quarter general and administrative expenses for 2021 were $5.3 million, compared to $2.0 million for the same period in 2020.

As of June 30, 2021, the total of cash and cash equivalents and investments was $365.1 million, exclusive of $35.0 million in the China JV.

About Kinnate

Kinnate is focused on the discovery and development of small molecule kinase inhibitors for difficult-to-treat, genomically defined cancers. Kinnate’s mission is to expand the reach of targeted therapeutics by developing products for underserved populations. Kinnate utilizes its deep expertise in structure-based drug discovery, translational research, and patient-driven precision medicine, which it refers to as the Kinnate Discovery Engine, to develop targeted therapies. Based in San Francisco and San Diego, California, the Kinnate team is composed of drug discovery experts supported by a distinguished group of scientific advisors. For more information, please visit www.kinnate.com.

Forward Looking Statements

This press release contains forward-looking statements that involve substantial risks and uncertainties. These forward-looking statements include, without limitation, statements regarding the development of our pipeline and the potential benefits of our drug discovery activities, the expected timing for our regulatory filings and enrollment and conduct of our clinical trials, the potential benefits and treatment indications of our product candidates and the expected expansion of our organization. Words such as “believes,” “anticipates,” “plans,” “expects,” “intends,” “will,” “goal,” “potential” and similar expressions are also intended to identify forward-looking statements. We have based these forward-looking statements largely on our current expectations and projections about future events and trends. Such expectations and projections may never materialize or may prove to be incorrect. These forward-looking statements are subject to a number of risks, uncertainties, assumptions and other factors, including risks related to operating as a preclinical-stage biopharmaceutical company with a limited operating history; our ability to raise additional capital to finance our operations; our ability to discover, advance through the preclinical and clinical development of, obtain regulatory approval for and commercialize our product candidates; the novel approach we are taking to discover and develop drugs; our ability to timely file and obtain approval of investigational new drug applications for our planned clinical trials; the potential for any clinical trial results to differ from our preclinical trial results; negative impacts of the COVID-19 pandemic on our business, including planned clinical trials and ongoing and planned preclinical trials; competition in our industry; regulatory developments in the United States and other countries; our ability to attract, hire and retain highly skilled executive officers and employees; difficulties in managing our growth; our ability to protect our intellectual property; reliance on third parties to conduct our preclinical studies and any future clinical trials, and to manufacture our product candidates; general economic and market conditions; and other risks.

These and other risks, uncertainties, assumptions and other factors are further described under the heading “Risk Factors” in our Quarterly Report on Form 10-Q for the quarterly period ended June 30, 2021 that we are concurrently filing with the Securities and Exchange Commission (the “SEC”), as well as in our subsequent filings we make with the SEC. New risk factors emerge from time to time and it is not possible for our management to predict all risk factors, nor can we assess the impact of all factors on our business or the extent to which any factor, or combination of factors, may cause actual results to differ materially from those contained in, or implied by, any forward-looking statements. Investors should not rely upon forward-looking statements as predictions of future events. Although we believe that the expectations reflected in the forward-looking statements are reasonable, we cannot guarantee future results, levels of activity, performance or achievements. Our forward-looking statements speak only as of the date of this release, and except as required by law, we undertake no obligation to update publicly any forward-looking statements for any reason in the future.


Contacts:

Investors:
Patti Bank
Westwicke, an ICR Company
415-513-1284
investors@kinnate.com

Media:
Colin Sanford
colin@bioscribe.com


Kinnate Biopharma Inc.
Condensed Consolidated Balance Sheets
(Unaudited)
(in thousands, except share and par value amounts)

   
June 30, 2021
   
December 31, 2020
 
Assets
           
Current assets:
           
Cash and cash equivalents
 
$
132,991
   
$
365,462
 
Cash at consolidated joint venture
   
35,011
     
-
 
Short-term investments
   
87,017
     
31,398
 
Prepaid expenses and other current assets
   
3,761
     
3,343
 
Total current assets
   
258,780
     
400,203
 
Property and equipment, net
   
286
     
368
 
Long-term investments
   
145,136
     
-
 
Restricted cash
   
371
     
-
 
Other non-current assets
   
90
     
-
 
Total assets
 
$
404,663
   
$
400,571
 
                 
Liabilities and Stockholders' Equity
               
Current liabilities:
               
Accounts payable
 
$
1,334
   
$
3,940
 
Accrued expenses
   
6,989
     
3,364
 
Total current liabilities
   
8,323
     
7,304
 
Commitments and contingencies
               
Redeemable noncontrolling interests
   
35,000
     
-
 
Stockholders’ equity:
               
Preferred stock, $0.0001 par value; 200,000,000 shares authorized
at June 30, 2021 and December 31, 2020; 0 shares outstanding
at June 30, 2021 and December 31, 2020
   
-
     
-
 
Common stock, $0.0001 par value; 1,000,000,000 shares authorized
at June 30, 2021 and December 31, 2020; 43,622,745 and 43,477,439
shares issued and outstanding at June 30, 2021 and December 31, 2020,
respectively
   
4
     
4
 
Additional paid-in capital
   
453,641
     
446,601
 
Accumulated other comprehensive loss
   
(74
)
   
(9
)
Accumulated deficit
   
(92,231
)
   
(53,329
)
Total stockholders’ equity
   
361,340
     
393,267
 
Total liabilities and equity
 
$
404,663
   
$
400,571
 


Kinnate Biopharma Inc.
Condensed Consolidated Statements of Operations and Comprehensive Loss
(Unaudited)
(in thousands, except share and per share amounts)

   
Three Months Ended June 30,
   
Six Months Ended June 30,
 
   
2021
   
2020
   
2021
   
2020
 
                         
Operating expenses:
                       
Research and development
 
$
16,242
   
$
5,579
   
$
28,908
   
$
8,777
 
General and administrative (includes related party amount of $92 for the three and six months ended June 30, 2020)
   
5,327
     
2,047
     
10,142
     
3,002
 
Total operating expenses
   
21,569
     
7,626
     
39,050
     
11,779
 
Loss from operations
   
(21,569
)
   
(7,626
)
   
(39,050
)
   
(11,779
)
Other income:
                               
Interest income
   
672
     
12
     
1,075
     
224
 
Other expense, net
   
(548
)
   
-
     
(927
)
   
-
 
Total other income, net
   
124
     
12
     
148
     
224
 
Net loss
   
(21,445
)
   
(7,614
)
   
(38,902
)
   
(11,555
)
Net loss attributable to redeemable noncontrolling interests
   
-
     
-
     
-
     
-
 
Net loss attributable to Kinnate
 
$
(21,445
)
 
$
(7,614
)
 
$
(38,902
)
 
$
(11,555
)
                                 
Weighted-average shares outstanding, basic and diluted
   
43,535,887
     
3,705,857
     
43,506,825
     
3,689,152
 
Net loss per share, basic and diluted
 
$
(0.49
)
 
$
(2.05
)
 
$
(0.89
)
 
$
(3.13
)
                                 
                                 
Comprehensive loss:
                               
Net loss
 
$
(21,445
)
 
$
(7,614
)
 
$
(38,902
)
 
$
(11,555
)
Other comprehensive (loss) income:
                               
Unrealized loss on investments
   
(34
)
   
-
     
(65
)
   
-
 
Total comprehensive loss
   
(21,479
)
   
(7,614
)
   
(38,967
)
   
(11,555
)
Comprehensive loss attributable to noncontrolling interests
   
-
     
-
     
-
     
-
 
Comprehensive loss attributable to Kinnate
 
$
(21,479
)
 
$
(7,614
)
 
$
(38,967
)
 
$
(11,555
)



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DE 001-39743 82-4566526 3611 Valley Centre Drive Suite 175 San Diego CA 92130 858 299-4699 false false false false Common Stock, $0.0001 par value per share KNTE NASDAQ true false XML 8 R1.htm IDEA: XBRL DOCUMENT v3.21.2
Document and Entity Information
Aug. 16, 2021
Cover [Abstract]  
Document Type 8-K
Amendment Flag false
Document Period End Date Aug. 16, 2021
Entity Registrant Name KINNATE BIOPHARMA INC.
Entity Incorporation, State or Country Code DE
Entity File Number 001-39743
Entity Tax Identification Number 82-4566526
Entity Address, Address Line One 3611 Valley Centre Drive
Entity Address, Address Line Two Suite 175
Entity Address, City or Town San Diego
Entity Address, State or Province CA
Entity Address, Postal Zip Code 92130
City Area Code 858
Local Phone Number 299-4699
Written Communications false
Soliciting Material false
Pre-commencement Tender Offer false
Pre-commencement Issuer Tender Offer false
Entity Emerging Growth Company true
Entity Ex Transition Period false
Entity Central Index Key 0001797768
Title of 12(b) Security Common Stock, $0.0001 par value per share
Trading Symbol KNTE
Security Exchange Name NASDAQ
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