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Plus Therapeutics Reports Second Quarter 2020 Financial and Business Results

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Plus Therapeutics, Inc. (Nasdaq: PSTV) reported a Q2 2020 net loss of $1.8 million, or $0.45 per share, significantly reduced from a loss of $9.1 million, or $20.67 per share, in Q2 2019. The company ended the quarter with $9.3 million in cash. Key developments include ongoing clinical trials for Rhenium NanoLiposomes (RNL™) aimed at treating recurrent glioblastoma, with preliminary data expected soon. The firm plans to finalize its Phase 2 trial plan and seek Orphan Drug Designation while exploring partnerships for its oncology portfolio.

Positive
  • Q2 2020 net loss decreased to $1.8 million from $9.1 million in Q2 2019.
  • Cash reserves improved to approximately $9.3 million.
  • 162,500 series U warrants were exercised, raising $0.36 million.
Negative
  • None.

AUSTIN, Texas, Aug. 10, 2020 (GLOBE NEWSWIRE) -- Plus Therapeutics, Inc. (Nasdaq: PSTV) (the “Company”), today announced financial and business results for its Second Quarter Fiscal Year 2020 ended June 30, 2020.

Q2 2020 net loss was $1.8 million, or $0.45 per share, including payments to NanoTx LLC of $0.78 million. Net cash used in operating activities for the six months ended June 30, 2020 was approximately $2.9 million. Plus Therapeutics ended Q2 2020 with approximately $9.3 million of cash and cash equivalents.

The Plus Therapeutics portfolio has three clinical-stage injectable drugs being developed on a unique nanotechnology platform designed to provide patient benefits through improved formulation and delivery innovation. The Company believes the platform can enable significant potential enhancements of safety, efficacy and convenience for oncology patients and their health providers compared to current standards of care.

The lead investigational drug in the Company’s licensed radiotherapeutic portfolio is Rhenium NanoLiposomes (RNL), a nanoliposome-encapsulated radionuclide for several cancer targets.  Initially being developed for the treatment of recurrent glioblastoma, RNL is being evaluated in the U.S. NIH/NCI-supported, multi-center ReSPECT™ Phase 1 dose-finding clinical trial (NCT01906385).  RNL is designed to safely, effectively, and conveniently deliver a very high dose of radiation directly into the brain tumor that is up to 25 times greater than that currently being given to recurrent glioblastoma patients using external beam radiation therapy.

H2 2020 Business Expansion Outlook

The first half of Fiscal Year 2020 marked the successful implementation of the Company’s refined development focus, initial pipeline expansion and optimized cost structure. In the second half of Fiscal Year 2020, the Company intends to focus on a number of additional business objectives and potential milestones:

  • Report preliminary RNL™ data from the ReSPECT Phase I dose finding trial in recurrent glioblastoma
  • Finalize RNL Phase 2/pivotal trial plan in recurrent glioblastoma
  • Seek RNL Orphan Drug Designation decisions from regulatory agencies
  • Complete evaluations of additional external and internal drug development candidates
  • Initiate IND-enabling RNL studies for additional indications
  • Explore partnership opportunities for RNL, DocePLUS and DoxoPLUS assets

“Following the close of our most recent in-licensing transaction, we have made steady progress in expediting the ReSPECT trial,” said Dr. Marc Hedrick, President and Chief Executive Officer of Plus Therapeutics.  “The second half of 2020 includes the prospect of further significant advancement for our RNL program-- and for the Company. We believe RNL has the potential of improving brain tumor therapy and that of other difficult to treat radiosensitive tumors.”

Q2 2020 Financial Highlights

  • Net cash used in operating activities was $2.9 million for the six months ended June 30, 2020, compared to $4.4 million during the same period in 2019.
  • In Q2 2020, 162,500 series U warrants were exercised, raising $0.36M.
  • Q2 2020 loss from continuing operations was $1.8 million, or $ 0.45 per share, compared to $2.3 million, or $5.12 per share for Q2 2019.
  • Q2 2020 net loss was $1.8 million, or $0.45 per share, compared to $9.1 million, or $20.67 per share, for Q2 2019, reflecting a loss from discontinued operations of $0 for Q2 2020 and $6.9 million in Q2 2019.

Investor Call Today at 5 p.m. EDT

The Company plans to hold a conference call and live audio webcast today at 5:00 PM Eastern Time to discuss its financial results and provide a general business update.

Event:Plus Therapeutics Second Quarter Fiscal Year 2020 Financial Results Conference Call and Webcast
Date:Monday, August 10, 2020
Time: 5:00 PM Eastern Time.
Live Call:Phone Number: (877) 402-3914; Conference ID:  5925129 
Live Webcast:https://event.on24.com/wcc/r/2402905/A6C80D40192BA72B1FDF935FEAFD7277
 Beginning two hours after the conclusion of the conference call, a replay will be available. 
Replay:http://ir.plustherapeutics.com/events/default.aspx

About Plus Therapeutics, Inc.

Plus Therapeutics (Nasdaq: PSTV) is a clinical-stage pharmaceutical company whose radiotherapeutic portfolio is concentrated on nanoliposome-encapsulated radionuclides for several cancer targets. Central to the Company’s drug development is a unique nanotechnology platform designed to reformulate, deliver and commercialize multiple drugs targeting rare cancers and other diseases. The platform is designed to facilitate new delivery approaches and/or formulations of safe and effective, injectable drugs, potentially enhancing the safety, efficacy and convenience for patients and healthcare providers. More information may be found at www.plustherapeutics.com and www.respect-trials.com

Cautionary Statement Regarding Forward-Looking Statements

This press release contains statements that may be deemed “forward-looking statements” within the meaning of U.S. securities laws. All statements in this press release other than statements of historical fact are forward-looking statements. These forward-looking statements may be identified by future verbs, as well as terms such as “will,” “believe,” “plan,” “can,” “enable,” “design,” “intend,” “potential,” “expect,” “estimate,” “project,” “prospect,” “target,” “focus,” “anticipate,” “could,” “should,” and similar expressions or the negatives thereof.  Such statements are based upon certain assumptions and assessments made by management in light of their experience and their perception of historical trends, current conditions, expected future developments and other factors they believe to be appropriate. These statements include, without limitation, statements regarding the following: the design and potential of the Plus Therapeutics portfolio to reformulate, deliver and commercialize multiple novel, proprietary drugs targeting rare cancers and other diseases and to facilitate new delivery approaches and/or formulations of safe and effective, injectable drugs; the Company’s belief as to the platform’s capacity to leverage new delivery approaches and/or formulations to enable significant potential enhancements of safety, efficacy and convenience for patients and healthcare providers; the potential of the Company’s portfolio generally, and the potential of RNL™ to safely and effectively deliver a dose of radiation directly to the tumor up to 25 times greater than that currently being given to patients using external beam radiation therapy; the Company’s belief as to the potential of RNL™ to improve brain tumor therapy and that of other difficult to treat radiosensitive tumors; the timing, status, outcome, and anticipated expansion of clinical trials for RNL™, including the planned initiation of an additional Phase 1 study and enrollment at additional sites, and the anticipated timing thereof; the Company’s business expansion outlook for the second half of 2020, including its intended focus on certain additional business expansion milestones; the Company’s expectations regarding the progress and prospect of advancement for the Company, RNL™, and the Company’s portfolio during the second half of 2020; and the potential impact of the COVID-19 pandemic on the Company and its clinical programs, operating results, and financial condition. The forward-looking statements included in this press release are subject to a number of risks and uncertainties that may cause actual results to differ materially from those discussed in such forward-looking statements.  These risks and uncertainties include, but are not limited to: the risk that the Company is not able to successfully develop product candidates that can leverage the U.S. FDA’s accelerated regulatory pathways; the early stage of the Company’s product candidates and therapies, the results of its research and development activities, including uncertainties relating to the clinical trials of its product candidates and therapies; the Company’s history of losses; the Company’s need for, and ability to raise, additional cash or obtain other sources of funding; the Company’s ability to: (a) obtain and maintain regulatory approvals, (b) continue as a going concern, (c) remain listed on the Nasdaq Capital Market, (d) to obtain or maintain sufficient levels of reimbursement for its tests, and (d) to repay or refinance some or all of its outstanding indebtedness; the outcome of the Company’s partnering/licensing efforts; market and economic conditions; the impact of the COVID-19 pandemic on the Company and the effectiveness of the efforts it has taken or may take in the future in response thereto; and additional risks described under the heading “Risk Factors” in the Company’s Securities and Exchange Commission filings, including in the Company’s annual and quarterly reports. There may be events in the future that the Company is unable to predict, or over which it has no control, and its business, financial condition, results of operations and prospects may change in the future. The Company assumes no responsibility to update or revise any forward-looking statements to reflect events, trends or circumstances after the date they are made unless the Company has an obligation under U.S. federal securities laws to do so.

 
 
PLUS THERAPEUTICS, INC.
CONSOLIDATED CONDENSED BALANCE SHEETS
(UNAUDITED)
(in thousands, except share and par value data)
 
  As of June 30,
2020
  As of December 31,
2019
 
Assets        
Current assets:        
Cash and cash equivalents $9,266  $17,552 
Accounts receivable  951   1,169 
Restricted cash     40 
Inventories, net  107   107 
Other current assets  469   957 
Total current assets  10,793   19,825 
         
Property and equipment, net  2,014   2,179 
Operating lease right-of-use assets  707   781 
Other assets  18   72 
Goodwill  372   372 
Total assets $13,904  $23,229 
Liabilities and Stockholders’ Equity        
Current liabilities:        
Accounts payable and accrued expenses $3,608  $3,279 
Operating lease liability  139   147 
Term loan obligations, net of discount  6,026   11,060 
Total current liabilities  9,773   14,486 
         
         
Noncurrent operating lease liability  589   646 
Warrant liability  242   6,929 
Other noncurrent liabilities     8 
Total liabilities  10,604   22,069 
         
Commitments and contingencies        
         
Stockholders’ equity:        
Preferred stock, $0.001 par value; 5,000,000 shares authorized; 1,959 shares issued
and outstanding at June 30, 2020 and December 31, 2019
      
Common stock, $0.001 par value; 100,000,000 shares authorized; 4,273,857 and
3,880,588 shares issued and outstanding at June 30, 2020 and December 31, 2019,
respectively
  4   4 
Additional paid-in capital  431,492   426,426 
Accumulated deficit  (428,196)  (425,270)
Total stockholders’ equity  3,300   1,160 
Total liabilities and stockholders’ equity $13,904  $23,229 


PLUS THERAPEUTICS, INC.
CONSOLIDATED CONDENSED STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS
(UNAUDITED)
(in thousands, except share and per share data)
 
  For the Three Months Ended June 30,  For the Six Months Ended June 30, 
  2020  2019  2020  2019 
Development revenues:                
Government contracts and other $185  $302  $303  $1,039 
Operating expenses:                
Research and development  327   1,289   1,268   2,715 
In process research and development acquired from NanoTx  781      781    
Sales and marketing  105   97   215   211 
General and administrative  1,324   875   2,832   2,237 
       Total operating expenses  2,537   2,261   5,096   5,163 
       Operating loss  (2,352)  (1,959)  (4,793)  (4,124)
                 
Other income (expense):                
Interest income  9   7   45   14 
Interest expense  (252)  (597)  (601)  (1,111)
Change in fair value of warrants  756   282   2,423   492 
      Total other income (expense)  513   (308)  1,867   (605)
Loss from continuing operations  (1,839)  (2,267)  (2,926)  (4,729)
Loss from discontinued operations     (6,880)     (7,568)
  Net loss $(1,839) $(9,147) $(2,926) $(12,297)
                 
Basic and diluted net loss per share attributable to common stockholders - continuing operations $(0.45) $(5.12) $(0.74) $(11.89)
Basic and diluted net loss per share attributable to common stockholders - discontinued operations $  $(15.55) $  $(19.02)
Net loss per share, basis and diluted $(0.45) $(20.67) $(0.74) $(30.91)
Basic and diluted weighted average shares used in calculating net loss per share attributable to common stockholders  4,053,242   442,512   3,967,392   397,827 
                 


PLUS THERAPEUTICS, INC.
CONSOLIDATED CONDENSED STATEMENTS OF CASH FLOWS
(UNAUDITED)
(in thousands)
 
  For the Six Months Ended June 30, 
  2020  2019 
Cash flows used in operating activities:        
Net loss $(2,926) $(12,297)
Adjustments to reconcile net loss to net cash used in operating activities:        
Depreciation and amortization  188   617 
Amortization of deferred financing costs and debt discount  275   257 
In process research and development acquired from NanoTx Therapeutics  781    
Noncash lease expenses  9   39 
Change in fair value of warrants  (2,423)  (492)
Share-based compensation expense  55   77 
Loss on sale of business     6,508 
Increases (decreases) in cash caused by changes in operating assets and liabilities:        
Accounts receivable  218   (28)
Inventories     235 
Other current assets  487   216 
Other assets  54   257 
Accounts payable and accrued expenses  371   108 
Deferred revenues     29 
Other long-term liabilities     54 
    Net cash used in operating activities  (2,911)  (4,420)
Cash flows provided by (used in) investing activities:        
Purchases of property and equipment  (23)  (6)
In process research and development acquired from NanoTx Therapeutics  (400)   
Proceeds from sale of business     5,637 
    Net cash provided by (used in) investing activities  (423)  5,631 
Cash flows used in financing activities:        
Principal payments of long-term obligations  (5,307)  (3,490)
Payment of financing lease liability  (51)  (28)
Proceeds from exercise of warrants  366    
Proceeds from sale of common stock, net     1,984 
    Net cash used in financing activities  (4,992)  (1,534)
    Effect of exchange rate changes on cash and cash equivalents     (4)
    Net decrease in cash and cash equivalents  (8,326)  (327)
Cash, cash equivalents, and restricted cash at beginning of period  17,592   5,301 
Cash, cash equivalents, and restricted cash at end of period $9,266  $4,974 
Supplemental disclosure of cash flows information:        
Cash paid during period for:        
Interest $372  $826 
Supplemental schedule of non-cash investing and financing activities:        
Common stock issued in payment for in process research and development $381    
         

Contact:
Plus Therapeutics, Inc. 
Andrew Sims
VP – Chief Financial Officer, Investor Relations
Phone: +1.619.333.4150
Email: ir@plustherapeutics.com
Corporate Website: plustherapeutics.com
Clinical Website:  respect-trials.com


FAQ

What were the financial results for Plus Therapeutics in Q2 2020?

Plus Therapeutics reported a net loss of $1.8 million, or $0.45 per share, for Q2 2020.

What is Rhenium NanoLiposomes (RNL) being developed for?

RNL is being developed for the treatment of recurrent glioblastoma.

What are Plus Therapeutics' cash reserves as of June 30, 2020?

As of June 30, 2020, Plus Therapeutics had approximately $9.3 million in cash and cash equivalents.

What is the expected timeline for RNL clinical trial data?

Preliminary data from the ReSPECT Phase I trial for RNL is expected to be reported in the second half of 2020.

What future plans does Plus Therapeutics have for RNL?

The company plans to finalize the RNL Phase 2 trial plan and seek Orphan Drug Designation from regulatory agencies.

PLUS THERAPEUTICS, Inc.

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