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Delcath Systems Announces Second Quarter 2021 Results

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Delcath Systems, Inc. (DCTH) reported its Q2 2021 financial results, showing product revenue of approximately $536K, up from $379K year-over-year. Despite this growth, the company incurred a net loss of $6.4M compared to a net income of $4.3M in Q2 2020. Key highlights include positive results from the FOCUS Phase III trial of HEPZATO™ KIT, with a 29.2% overall response rate in treated patients. Additionally, Delcath's CHEMOSAT® received updated guidance from the UK's National Institute for Health and Care Excellence, enhancing treatment funding prospects.

Positive
  • Q2 product revenue increased to approximately $536K from $379K year-over-year.
  • Positive efficacy results from the FOCUS Phase III trial of HEPZATO™ KIT were presented at ASCO.
  • CHEMOSAT® received updated guidance from the UK's National Institute for Health and Care Excellence, improving funding access.
  • The company entered a $20M debt facility with Avenue Venture Opportunities Fund, providing critical funding.
Negative
  • Net loss of $6.4M in Q2 2021 compared to a net income of $4.3M in Q2 2020.
  • Total operating expenses increased to $6.8M, up from $4.5M in the prior year quarter.

NEW YORK, Aug. 10, 2021 (GLOBE NEWSWIRE) -- Delcath Systems, Inc. (Nasdaq: DCTH), an interventional oncology company focused on the treatment of rare primary and metastatic cancers of the liver, today reported business highlights and financial results for the second quarter ended June 30, 2021.

Recent Business Highlights

During and since the second quarter the company:

  • Had positive efficacy results presented from its FOCUS Phase III trial of HEPZATO™ KIT (melphalan hydrochloride for injection/hepatic delivery system) in patients with liver dominant metastatic ocular melanoma (mOM) at the American Society of Clinical Oncology (ASCO) Annual Meeting. The oral presentation by the study’s Lead Investigator, Dr. Jonathan Zager, Chief Academic Officer, Chair, USF Department of Oncologic Sciences, Moffitt Cancer Center, included data based on 79 of 91 treated HEPZATO patients showing an overall response rate of 29.2% with a 95% confidence interval lower bound of 20%. Given the magnitude by which the lower bound exceeded the 8.3% prespecified threshold for success, the primary endpoint of the trial has been met regardless of the outcome of patients who have not yet been evaluated. Patient level response data were also presented for this same patient set, indicating that 44% of evaluable patients in the HEPZATO arm had a 30% or greater reduction in target tumor lesions at one or more time points versus 17% for patients enrolled in the Best Alternative Care arm.
  • Announced that the United Kingdom’s National Institute for Health and Care Excellence, has updated its guidance for the Delcath CHEMOSAT® Hepatic Delivery System for Melphalan (CHEMOSAT) in the treatment of patients with metastases in the liver from Ocular Melanoma. Under this designation, private insurance may be more likely to fund treatment with CHEMOSAT, some regional funding may be more accessible, and a process is now available to seek national reimbursement.
  • Entered into a debt facility with Avenue Venture Opportunities Fund, L.P. providing up to $20 million with an initial $15 million funded at close
  • Was added to the Russell Microcap® Index. Membership in the Russell Microcap® Index, which remains in place for one year, means automatic inclusion in the appropriate growth and value style indexes. FTSE Russell determines membership for its Russell indexes primarily by objective, market-capitalization rankings and style attributes.

“During the quarter we announced new patient level data at ASCO that further strengthens the case that HEPZATO would offer a compelling clinical benefit to patients were it approved by the FDA,” said Gerard Michel, CEO of Delcath. “With additional capital from the just closed transaction with Avenue Venture Opportunities Fund, Delcath has the required resources to accomplish its strategic priorities – the filing of the HEPZATO NDA in early 2022, preparing for the subsequent US launch when approved, and expanding the development of HEPZATO into additional areas of high unmet need.”

First Quarter 2021 Financial Results:

Income Statement Highlights.

Product revenue for the three months ended June 30, 2021 was approximately $536 thousand, compared to $379 thousand for the prior year period from our sales of CHEMOSAT procedures in Europe. Selling, general and administrative expenses were approximately $3.3 million compared to $2.3 million in the prior year quarter. Research and development expenses for the quarter were $3.5 million compared to $2.2 million in the prior year quarter. Total operating expenses for the quarter were $6.8 million compared with $4.5 million in the prior year quarter. Expenses for the quarter included approximately $1.6 million of stock option expense compared to no stock option expense in the prior year quarter.

The company recorded a net loss for the three months ended June 30, 2021, of $6.4 million, compared to a net income of $4.3 million for the same period in 2020

Balance Sheet Highlights.

On June 30, 2021, we had cash, cash equivalents and restricted cash totaling $19.4 million, as compared to cash, cash equivalents and restricted cash totaling $16.2 million at June 30, 2020. During the three months ended June 30, 2021 and June 30, 2020, we used $11.7 million and $13.1 million, respectively, of cash in our operating activities.

On August 6th, we closed a $20 million venture debt financing transaction with Avenue Venture Opportunities Fund ("Avenue Venture Fund"). The initial tranche of the Loan is $15 million, including $4 million which has been funded into a restricted account and will be released upon achievement of certain milestones. The Company may request an additional $5 million of gross proceeds between October 1, 2022 and December 31, 2022, which will be funded at Avenue Venture Fund’s discretion.

Also, on August 6th, we amended two existing convertible notes through an extension of the term of the notes until 2024 and lowered the conversion factor in consideration for the notes becoming subordinate to the Avenue Venture Fund debt.

Additional details concerning the Avenue Venture Fund facility and modification of the existing convertible notes will be contained in the company's Current Report on Form 8-K to be filed with the Securities and Exchange Commission.

Conference Call Information

To participate in this event, dial approximately 5 to 10 minutes before the beginning of the call.

Date: August 10, 2021
Time: 8:30 AM Eastern Time
Toll Free: 877-545-0523; Entry Code: 148562
International: 973-528-0016; Entry Code: 148562

The call will also be available over the Internet and accessible at:

https://www.webcaster4.com/Webcast/Page/2475/42376

About Delcath Systems, Inc.

Delcath Systems, Inc. is an interventional oncology company focused on the treatment of primary and metastatic liver cancers. The company’s proprietary percutaneous hepatic perfusion (PHP) system is designed to administer high-dose chemotherapy to the liver while controlling systemic exposure and associated side effects. In the United States, the PHP system is being developed under the tradename HEPZATO KIT (melphalan hydrochloride for injection/hepatic delivery system), or HEPZATO, and is considered a combination drug and device product regulated by the United States Food and Drug Administration (FDA).

In Europe, the PHP system is regulated as a Class IIb medical device and is approved for sale under the trade name CHEMOSAT Hepatic Delivery System for Melphalan, or CHEMOSAT, where it has been used at major medical centers to treat a wide range of cancers of the liver. CHEMOSAT is being marketed under an exclusive licensing agreement with medac GmbH, a privately held multi-national pharmaceutical company headquartered in Germany that specializes in the treatment and diagnosis of oncological, urological and autoimmune diseases.

Safe Harbor / Forward-Looking Statements

The Private Securities Litigation Reform Act of 1995 provides a safe harbor for forward-looking statements made by the Company or on its behalf. This news release contains forward-looking statements, which are subject to certain risks and uncertainties that can cause actual results to differ materially from those described. Factors that may cause such differences include, but are not limited to, uncertainties relating to: the timing and results of the Company’s clinical trials, including without limitation the mOM and ICC clinical trial programs, as well as the receipt of additional data and the performance of additional analyses with respect to the mOM clinical trial, our determination whether to continue the ICC clinical trial program or to focus on other alternative indications, and timely monitoring and treatment of patients in the global Phase 3 mOM clinical trial and the impact of the COVID-19 pandemic on the completion of our clinical trials; the impact of the presentations at major medical conferences and future clinical results consistent with the data presented; approval of Individual Funding Requests for reimbursement of the CHEMOSAT procedure; the impact, if any, of ZE reimbursement on potential CHEMOSAT product use and sales in Germany; clinical adoption, use and resulting sales, if any, for the CHEMOSAT system to deliver and filter melphalan in Europe including the key markets of Germany and the UK; the Company’s ability to successfully commercialize the HEPZATO KIT/CHEMOSAT system and the potential of the HEPZATO KIT/CHEMOSAT system as a treatment for patients with primary and metastatic disease in the liver; our ability to obtain reimbursement for the CHEMOSAT system in various markets; approval of the current or future HEPZATO KIT/CHEMOSAT system for delivery and filtration of melphalan or other chemotherapeutic agents for various indications in the U.S. and/or in foreign markets; actions by the FDA or foreign regulatory agencies; the Company’s ability to successfully enter into strategic partnership and distribution arrangements in foreign markets and the timing and revenue, if any, of the same; uncertainties relating to the timing and results of research and development projects; and uncertainties regarding the Company’s ability to obtain financial and other resources for any research, development, clinical trials and commercialization activities. These factors, and others, are discussed from time to time in our filings with the Securities and Exchange Commission. You should not place undue reliance on these forward-looking statements, which speak only as of the date they are made. We undertake no obligation to publicly update or revise these forward-looking statements to reflect events or circumstances after the date they are made.

Contact:

Delcath Investor Relations

Email: investorrelations@delcath.com

Hayden IR

James Carbonara
(646)-755-7412
james@haydenir.com


DELCATH SYSTEMS, INC.
Condensed Consolidated Balance Sheets
(Unaudited)
(in thousands, except share and per share data)

  June 30,  December 31, 
  2021  2020 
Assets        
Current assets        
Cash and cash equivalents $19,274  $28,575 
Restricted cash  151   181 
Accounts receivable, net  75   57 
Inventories  1,221   855 
Prepaid expenses and other current assets  2,185   2,670 
Total current assets  22,906   32,338 
Property, plant and equipment, net  1,361   1,351 
Right-of-use assets  650   946 
Total assets $24,917  $34,635 
         
Liabilities and Stockholders' Equity        
Current liabilities        
Accounts payable $1,224  $1,774 
Accrued expenses  3,621   5,241 
Deferred revenue, current  509   525 
Lease liabilities, current  387   495 
Convertible notes payable, current     2,000 
Total current liabilities  5,741   10,035 
Deferred revenue, non-current  1,754   2,072 
Lease liabilities, non-current  263   450 
Convertible notes payable, non-current  2,000    
Total liabilities  9,758   12,557 
         
Commitments and contingencies (Note 11)      
         
Stockholders' equity        
Preferred stock, $.01 par value; 10,000,000 shares authorized; 11,707 and 20,631 shares
issued and outstanding at June 30, 2021, and December 31, 2020, respectively
      
Common stock, $.01 par value; 40,000,000 shares authorized; 7,349,777 and
5,996,101 shares issued and outstanding at June 30, 2021, and
December 31, 2020, respectively
  74   60 
Additional paid-in capital  423,660   417,449 
Accumulated deficit  (408,504)  (395,327)
Accumulated other comprehensive loss  (71)  (104)
Total stockholders' equity  15,159   22,078 
Total liabilities and stockholders' equity $24,917  $34,635 
         

DELCATH SYSTEMS, INC.
Condensed Consolidated Statements of Operations and Comprehensive Loss
(Unaudited)

(in thousands, except share and per share data) 
                
                
 Three months ended
June 30,
  Six months ended
June 30,
 
 2021  2020  2021  2020 
Product revenue$398  $262  $659  $437 
Other revenue 138   117   265   235 
Cost of goods sold (202)  (168)  (314)  (246)
Gross profit 334   211   610   426 
                
Operating expenses:               
Research and development expenses 3,497   2,223   7,204   5,197 
Selling, general and administrative expenses 3,288   2,257   6,584   4,573 
Total operating expenses 6,785   4,480   13,788   9,770 
Operating loss (6,451)  (4,269)  (13,178)  (9,344)
                
Change in fair value of the warrant liability, net          (2,832)
Interest expense, net (40)  (52)  (81)  (88)
Other income 61   46   82   128 
Net loss (6,430)  (4,275)  (13,177)  (12,136)
                
Deemed dividend for triggering of warrant down round feature    (55)     (55)
Net loss attributable to common stockholders$(6,430) $(4,330) $(13,177) $(12,191)
                
Net loss$(6,430) $(4,275) $(13,177) $(12,136)
Other comprehensive (loss) income:               
Foreign currency translation adjustments (61)  (1)  33   65 
Total other comprehensive loss$(6,491) $(4,276) $(13,144) $(12,071)
                
Common share data:               
Basic loss per common share$(0.96) $(1.90) $(2.00) $(10.40)
Diluted loss per common share$(0.96) $(1.90) $(2.00) $(10.40)
                
Weighted average number of basic shares outstanding 6,681,369   2,273,187   6,589,655   1,171,994 
Weighted average number of diluted shares outstanding 6,681,369   2,273,187   6,589,655   1,171,994 

 


FAQ

What were Delcath Systems' Q2 2021 financial results?

Delcath reported Q2 2021 product revenue of approximately $536K, a net loss of $6.4M, and total operating expenses of $6.8M.

What positive news did Delcath announce in August 2021?

Delcath announced positive efficacy results from its FOCUS Phase III trial of HEPZATO™ KIT and received updated CHEMOSAT® guidance from the UK's NICE.

What is the significance of the debt facility entered by Delcath?

Delcath secured a $20 million debt facility with Avenue Venture Opportunities Fund, helping support its strategic priorities.

How did Delcath's trial results impact its stock symbol DCTH?

The positive results from the FOCUS trial could enhance investor confidence in DCTH, potentially influencing stock performance.

What is the expected timeline for HEPZATO NDA filing?

Delcath aims to file the HEPZATO NDA in early 2022.

Delcath Systems Inc

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