6-K

 

 

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

of the Securities Exchange Act of 1934

Date of Report: August 31, 2020

Commission File Number: 001-39307

 

 

Legend Biotech Corporation

(Exact Name of Registrant as Specified in its Charter)

 

 

2101 Cottontail Lane

Somerset, New Jersey 08873

(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):  ☐

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):  ☐

 

 

 


Earnings Release

On August 28, 2020, Legend Biotech Corporation (the “Company”) issued a press release regarding its unaudited financial results for the three and six months ended June 30, 2020 and recent business highlights, which is attached to this Form 6-K as Exhibit 99.1.

EXHIBIT INDEX

 

Exhibit

  

Title

99.1    Press Release, dated August 28, 2020.


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, thereunto duly authorized.

 

    LEGEND BIOTECH CORPORATION
    (Registrant)
August 31, 2020     By:  

/s/ Ying Huang

      Ying Huang, Ph.D.
      Chief Financial Officer
EX-99.1

Exhibit 99.1

 

LOGO

Legend Biotech Reports Second Quarter 2020 Financial Results

SOMERSET, N.J.—(BUSINESS WIRE)—August 28, 2020—Legend Biotech Corporation (NASDAQ: LEGN) (Legend Biotech), a global clinical-stage biopharmaceutical company engaged in the discovery and development of novel cell therapies for oncology and other indications, today reported financial results for the quarter ended June 30, 2020.

“Legend Biotech continues to execute on our corporate strategy, advancing the development of our lead product candidate, ciltacabtagene autoleucel (cilta-cel), in collaboration with Janssen Biotech, Inc. as well as our other pipeline programs,” said Frank Zhang, Ph.D., Chief Executive Officer and Chairman of the Board of Legend Biotech. “We look forward to presenting data from the CARTITUDE-1 study at a major medical conference in the second half of 2020.”

Second Quarter 2020 & Recent Highlights

 

   

Collaborative Research and License Agreement with Noile-Immune Biotech. On April 27, 2020, Legend Biotech entered into a collaborative research and license agreement with Noile-Immune Biotech Inc. pursuant to which Legend Biotech obtained a license to develop and commercialize next-generation CAR-T and/or TCR-T cell therapies incorporating Noile-Immune’s PRIME (proliferation-inducing and migration-enhancing) technology for up to two targets for all indications.

 

   

Updated Results from Janssen sponsored Phase 1b/2 CARTITUDE-1 study. On May 13, 2020, Legend Biotech announced positive follow up data (median of 11.5 months) from the Phase 1b portion of the CARTITUDE-1 study evaluating cilta-cel1 (JNJ-4528) in heavily pretreated patients with relapsed or refractory multiple myeloma (RRMM).

 

   

Appointment of Three New Directors. In May 2020, Dr. Corazon (Corsee) Dating Sanders, Dr. Darren Ji, and Mr. Philip Yau joined Legend Biotech’s Board of Directors.

 

   

Successful Initial Public Offering. On June 9, 2020, Legend Biotech successfully completed its initial public offering for total gross proceeds of approximately $487.3 million.

 

   

Appointment of Dr. Frank Zhang as CEO. On August 1, 2020, the Board of Directors of Legend Biotech appointed Dr. Frank Zhang to serve as Chief Executive Officer, succeeding Dr. Yuan Xu upon her resignation.

 

   

First Breakthrough Therapy Designation from China CDE. On August 5, 2020, Legend Biotech announced that the China Center for Drug Evaluation (“CDE”), National Medical Products Administration recommended Breakthrough Therapy Designation (“BTD”) for cilta-cel for the treatment of adults with relapsed/refractory multiple myeloma. The designation was granted on August 13, 2020, making cilta-cel the first investigational product to obtain BTD in China.

 

1 

Ciltacabtagene autoleucel (cilta-cel) refers to both JNJ-4528 (the identifier for the investigational product being studied outside of China) and LCAR-B38M CAR-T cell (the identifier for the investigational product being studied in China), both of which identify the same CAR-T cell therapy.


Key Upcoming Milestones

 

   

Legend Biotech, in collaboration with Janssen Biotech, Inc., anticipates the presentation of data from the CARTITUDE-1 study at a major medical conference in the second half of 2020.

 

   

Janssen Biotech, Inc., Legend Biotech’s collaboration partner, expects to initiate the BLA filing for cilta-cel to the U.S. FDA by the end of 2020 and also expects that a marketing authorization application will be submitted to the European Medicines Agency (“EMA”) in early 2021.

 

   

Legend Biotech expects to use the data from CARTIFAN-1 in support of a regulatory submission for approval in China in 2021.

 

   

Legend Biotech intends to submit an IND application for LB1901 in relapsed or refractory T cell Lymphoma (“TCL”) in the second half of 2020.

The extent to which the COVID-19 may impact our business and clinical trials is highly uncertain and cannot be predicted with confidence, such as the ultimate geographic spread of the disease, the duration of the outbreak and social distancing regulations, travel restrictions, business closures or business disruptions and the effectiveness of actions taken in the United States and other countries to contain and treat the disease.

Financial Results for the Quarter Ended June 30, 2020

Cash and Cash Equivalents:

As of June 30, 2020, Legend Biotech had approximately $562.4 million of cash and cash equivalents and approximately $75.6 million in time deposits.

Revenue

Revenue for the three months ended June 30, 2020 was $11.6 million compared to $10.1 million for the three months ended June 30, 2019. This increase of $1.5 million was primarily due to additional milestone payments from Janssen Biotech, Inc. that were achieved in late 2019, which resulted in additional consideration being allocated to steering committee service for the three month ended June 30, 2020. Revenue for the three months ended June 30, 2020 and June 30, 2019 consisted of recognition of upfront and milestone payments allocated to steering committee service pursuant to the license and collaboration agreement with Janssen Biotech, Inc. Legend Biotech has not generated any revenue from product sales to date.

Research and Development Expenses

Research and development expenses for the three months ended June 30, 2020 were $53.6 million compared to $32.6 million for the three months ended June 30, 2019. This increase of $21.0 million was primarily due to a higher number of clinical trials, a higher number of patients enrolled in those trials and a higher number of research and development product candidates in the three months ended June 30, 2020.

 

2


Administrative Expenses

Administrative expenses for the three months ended June 30, 2020 were $4.5 million compared to $1.6 million for the three months ended June 30, 2019. This increase of $2.9 million was primarily due to Legend Biotech’s expansion of supporting administrative functions to aid continued research and development activities.

Selling and Distribution Expenses

Selling and distribution expenses for the three months ended June 30, 2020 were $9.6 million compared to $5.0 million for the three months ended June 30, 2019. This increase of $4.6 million was primarily due to increased costs associated with commercial preparation activities for cilta-cel.

Other Income and Gains

Other income and gains for the three months ended June 30, 2020 was $1.3 million compared to $1.2 million for the three months ended June 30, 2019.

Fair Value Loss of Convertible Redeemable Preferred Shares

For the three months ended June 30, 2020, Legend Biotech reported a one-time non-cash charge of $80.0 million caused by changes of fair value of Series A convertible redeemable preferred shares (Series A Preferred Shares). Upon listing on the Nasdaq Global Market, all outstanding Series A Preferred Shares were converted into ordinary shares of Legend Biotech and all accrued but unpaid dividends were settled in the form of ordinary shares of Legend Biotech.

Loss for the Period

For the three months ended June 30, 2020, net loss was $134.9 million, or $0.63 per share, compared to a net loss of $28.8 million, or $0.14 per share, for the three months ended June 30, 2019.

About Legend Biotech

Legend Biotech is a global clinical-stage biopharmaceutical company engaged in the discovery and development of novel cell therapies for oncology and other indications. Our team of over 700 employees across the United States, China and Europe, along with our differentiated technology, global development, and manufacturing strategies and expertise, provide us with the strong potential to discover, develop, and manufacture best-in-class cell therapies for patients in need.

We are engaged in a strategic collaboration with Janssen Biotech, Inc. to develop and commercialize our lead product candidate, ciltacabtagene autoleucel, an investigational BCMA-targeted CAR-T cell therapy for patients living with multiple myeloma. This candidate is currently being studied in registrational clinical trials.

Cautionary Note Regarding Forward-Looking Statements

Statements in this press release about future expectations, plans and prospects, as well as any other statements regarding matters that are not historical facts, constitute “forward-looking statements” within the meaning of The Private Securities Litigation Reform Act of 1995. These statements include, but are not limited to, statements relating to Legend Biotech’s strategies and objectives; the anticipated timing of, and ability to progress, clinical trials; the ability to make, and the timing of, regulatory submissions in the United States, Europe and Asia, including the BLA filing for

 

3


cilta-cel to the U.S. FDA, the submission of a marketing authorization application for cilta-cel to the EMA, and the submission of an IND LB1901 in relapsed or refractory TCL; the ability to generate, analyze and present data from clinical trials; patient enrollment; and the potential benefits of our product candidates. The words “anticipate,” “believe,” “continue,” “could,” “estimate,” “expect,” “intend,” “may,” “plan,” “potential,” “predict,” “project,” “should,” “target,” “will,” “would” and similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. Actual results may differ materially from those indicated by such forward-looking statements as a result of various important factors, including the factors discussed in the “Risk Factors” section of the prospectus filed with the Securities and Exchange Commission on June 8, 2020. Any forward-looking statements contained in this press release speak only as of the date hereof, and Legend Biotech specifically disclaims any obligation to update any forward-looking statement, whether as a result of new information, future events or otherwise. Readers should not rely upon the information on this page as current or accurate after its publication date.

 

4


LEGEND BIOTECH CORPORATION

UNAUDITED INTERIM CONDENSED

CONSOLIDATED STATEMENTS OF PROFIT OR LOSS

FOR THE THREE AND SIX MONTHS ENDED JUNE 30, 2020 AND 2019

 

     Three months ended
June 30
    Six months ended
June 30
 
(in thousands, US$, except share and per share data)    2020
(unaudited)
    2019
(unaudited)
    2020
(unaudited)
    2019
(unaudited)
 

REVENUE

     11,600       10,087       23,146       20,140  

Other income and gains

     1,265       1,221       3,796       4,073  

Research and development expenses

     (53,567     (32,640     (101,570     (53,929

Administrative expenses

     (4,508     (1,607     (7,938     (2,712

Selling and distribution expenses

     (9,557     (5,030     (16,102     (7,786

Other expenses

     (37     (478     (82     (625

Fair value loss of convertible redeemable preferred shares

     (79,984     —         (79,984     —    

Finance costs

     (88     (19     (4,079     (57
  

 

 

   

 

 

   

 

 

   

 

 

 

LOSS BEFORE TAX

     (134,876     (28,466     (182,813     (40,896
  

 

 

   

 

 

   

 

 

   

 

 

 

Income tax (expense)/credit

     —         (336     3,709       (336
  

 

 

   

 

 

   

 

 

   

 

 

 

LOSS FOR THE PERIOD

     (134,876     (28,802     (179,104     (41,232
  

 

 

   

 

 

   

 

 

   

 

 

 

Attributable to:

        

Equity holders of the parent

     (134,876     (28,802     (179,104     (41,232
  

 

 

   

 

 

   

 

 

   

 

 

 

LOSS PER SHARE ATTRIBUTABLE TO ORDINARY EQUITY HOLDERS OF THE PARENT

        

Ordinary shares—basic

     (0.63     (0.14     (0.86     (0.21
  

 

 

   

 

 

   

 

 

   

 

 

 

Ordinary shares—diluted

     (0.63     (0.14     (0.86     (0.21
  

 

 

   

 

 

   

 

 

   

 

 

 

Ordinary shares used in loss per share computation:

        

Ordinary shares—basic

     215,551,887       200,000,000       207,775,944       200,000,000  
  

 

 

   

 

 

   

 

 

   

 

 

 

Ordinary shares—diluted

     215,551,887       200,000,000       207,775,944       200,000,000  
  

 

 

   

 

 

   

 

 

   

 

 

 

 

5


LEGEND BIOTECH CORPORATION

UNAUDITED INTERIM CONDENSED CONSOLIDATED STATEMENTS OF FINANCIAL POSITION

AS AT JUNE 30, 2020 AND DECEMBER 31, 2019

 

     June 30, 2020
(Unaudited)
     December 31,
2019
 
(in thousands, US$)              

NON-CURRENT ASSETS

     

Property, plant and equipment

     88,589        70,079  

Advance payments for property, plant and equipment

     2,121        665  

Right-of-use assets

     7,786        9,348  

Intangible assets

     978        519  
  

 

 

    

 

 

 

Total non-current assets

     99,474        80,611  
  

 

 

    

 

 

 

CURRENT ASSETS

     

Inventories

     1,668        1,157  

Trade receivables

     —          29,991  

Prepayments, other receivables and other assets

     33,517        16,777  

Pledged short-term deposits

     256        256  

Time deposits

     75,559        75,559  

Cash and cash equivalents

     562,391        83,364  
  

 

 

    

 

 

 

Total current assets

     673,391        207,104  
  

 

 

    

 

 

 

Total assets

     772,865        287,715  
  

 

 

    

 

 

 

CURRENT LIABILITIES

     

Trade and notes payables

     6,976        9,586  

Other payables and accruals

     60,429        70,854  

Lease liabilities

     1,314        1,027  

Contract liabilities

     46,312        46,294  
  

 

 

    

 

 

 

Total current liabilities

     115,031        127,761  
  

 

 

    

 

 

 

NON-CURRENT LIABILITIES

     

Contract liabilities

     254,714        277,765  

Lease liabilities

     2,119        5,058  
  

 

 

    

 

 

 

Total non-current liabilities

     256,833        282,823  
  

 

 

    

 

 

 

Total liabilities

     371,864        410,584  
  

 

 

    

 

 

 

EQUITY

     

Share capital

     26        20  

Reserves/(deficits)

     400,975        (122,889
  

 

 

    

 

 

 

Total ordinary shareholders’ equity/(deficit)

     401,001        (122,869
  

 

 

    

 

 

 

Total equity/(deficit)

     401,001        (122,869
  

 

 

    

 

 

 

Total liabilities and equity

     772,865        287,715  
  

 

 

    

 

 

 

 

6


LEGEND BIOTECH CORPORATION

UNAUDITED INTERIM CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS

FOR THE THREE AND SIX MONTHS ENDED JUNE 30, 2020 AND 2019

 

     Three months ended
June 30
    Six months ended
June 30
 
(in thousands, US$)    2020
(Unaudited)
    2019
(Unaudited)
    2020
(Unaudited)
    2019
(Unaudited)
 

LOSS BEFORE TAX

     (134,876     (28,466     (182,813     (40,896

CASH FLOWS USED IN OPERATING ACTIVITIES

     (56,885     (38,766     (102,681     (43,025

CASH FLOWS USED IN INVESTING ACTIVITIES

     (9,212     (36,031     (26,711     (150,909

CASH FLOWS FROM/(USED IN) FINANCING ACTIVITIES

     459,803       (7,177     608,558       21,500  
  

 

 

   

 

 

   

 

 

   

 

 

 

NET INCREASE/(DECREASE) IN CASH AND CASH EQUIVALENTS

     393,706       (81,974     479,166       (172,434

Effect of foreign exchange rate changes, net

     (112     (16     (139     (11

Cash and cash equivalents at beginning of the period

     168,797       119,711       83,364       210,166  
  

 

 

   

 

 

   

 

 

   

 

 

 

CASH AND CASH EQUIVALENTS AT END OF THE PERIOD

     562,391       37,721       562,391       37,721  
  

 

 

   

 

 

   

 

 

   

 

 

 

ANALYSIS OF BALANCES OF CASH AND CASH EQUIVALENTS

        

Cash and bank balances

     638,206       149,032       638,206       149,032  
  

 

 

   

 

 

   

 

 

   

 

 

 

Less: Pledged short-term deposits

     256       250       256       250  

Time deposits

     75,559       111,061       75,559       111,061  

Cash and cash equivalents as stated in the statement of financial position

     562,391       37,721       562,391       37,721  

Cash and cash equivalents as stated in the statement of cash flows

     562,391       37,721       562,391       37,721  

 

7


Media and Investor Relations:

Jessie Yeung, Head of Corporate Finance and Investor

Relations, Legend Biotech jessie.yeung@legendbiotech.com or

investor@legendbiotech.com

Source: Legend Biotech

 

8