Plus Therapeutics Reports First Quarter 2021 Financial Results and Business HighlightsManagement to host conference call today at 5:00 pm ET
AUSTIN, Texas, April 22, 2021 (GLOBE NEWSWIRE) -- Plus Therapeutics, Inc. (Nasdaq: PSTV) (the “Company”), a clinical-stage pharmaceutical company developing novel, targeted therapies for rare and difficult to treat cancers, today announced financial results for the first quarter ended March 31, 2021, and provided an overview of recent business highlights.
The Company’s lead investigational drug is Rhenium NanoLiposome (RNL™), a radiotherapy in development for several rare cancer targets, including recurrent glioblastoma (GBM). RNL™, currently being evaluated in the U.S. multi-center ReSPECT™ Phase 1 dose-finding clinical trial, is designed to safely, effectively, and conveniently deliver a very high dose of radiation directly to brain tumors.
“In the first quarter of 2021, we made meaningful progress in critical areas including advancing our drug development and manufacturing activities, refining our clinical understanding of RNL™ behavior in the glioblastoma patients and in seeking FDA feedback on potential new clinical indications for RNL™,” said Marc H. Hedrick M.D., President and Chief Executive Officer of Plus Therapeutics.
First Quarter 2021 Clinical Highlights
Company highlights during the first quarter of 2021 included:
- Entering into a master services agreement (MSA) with Piramal Pharma Solutions for the development, manufacture, and supply of RNL™ intermediate drug product.
- Completing the 6th dose escalation cohort, with 18 patients treated in ReSPECT™, with concomitant increases in both RNL™ drug volume and radiation dose.
- Beginning treatment in an expansion cohort at the 6th dose with higher drug flow rates and faster drug infusion times.
- Submitting 2 RNL™ pre-IND meeting briefing packages to the U.S. Food and Drug Administration (FDA) for treatment of leptomeningeal metastases and pediatric brain cancers, specifically ependymoma, high-grade glioma, and diffuse intrinsic pontine glioma.
Expected Upcoming Clinical Milestones and Events for 2021
In upcoming quarters in 2021, the Company intends to focus on a number of additional business objectives and potential milestones:
- Complete enrollment of the ReSPECT™ Phase 1 trial for RNL™ in recurrent glioblastoma.
- Complete pivotal trial planning in conjunction with FDA feedback for RNL™ in recurrent glioblastoma.
- Complete a pre-IND meeting with the FDA, execute IND-enabling studies, if needed, and move into clinical trials for new RNL™ indications.
- Continue development and evaluation of additional external and internal drug development candidates to expand the drug development pipeline.
- Continue to explore partnership opportunities for three clinical-stage investigational drugs: RNL™, DocePLUS™ and generic DoxoPLUS™.
First Quarter 2021 Financial Results
- As of March 31, 2021, the Company’s cash balance was $14.4 million, compared to $8.3 million as of December 31, 2020.
- Total operating expenses for the first quarter of 2021 was $2.5 million, compared to total operating expenses of $2.56 million for the same quarter in 2020.
- Net loss for the first quarter of 2021 was $2.7 million, or $(0.33) per share, compared to a net loss of $1.1 million, or $(0.28) per share, for the same quarter in 2020. The net loss was consistent year on year when excluding the book gains on the warrants reported in Q1 2020. Remeasurement of warrant liabilities was no longer required for Series U warrants that were amended in Q2 and Q3 2020 and reclassified to equity.
First Quarter 2021 Results Conference Call
The Company will hold a conference call and live audio webcast at 5:00 p.m. Eastern Time today to discuss its financial results and provide a general business update.
|Event:||Plus Therapeutics First Quarter 2021 Results Conference Call|
|Date:||Thursday, April 22, 2021|
|Time:||5:00 p.m. Eastern Time|
|Live Call:||877-402-3914 (toll free); 631-865-5294 (Intl.); Conference ID: 3084418|
The webcast can be accessed live via the investor section of the Plus Therapeutics website at ir.plustherapeutics.com/events and will be available for replay beginning two hours after the conclusion of the conference call.
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 PlusTherapeutics.com and 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 potential of the Company’s in-licensed portfolio of investigational drugs; the Company’s intent to advance its CNS oncology portfolio through the clinical development process; the ability of RNL to safely, effectively and conveniently deliver a very high dose of radiation directly into the brain tumor; anticipated benefits of strategic collaborations and license agreements, intellectual property, FDA approval process and government regulation; and the Company’s anticipated milestones and events, including with respect to additional sites, enrollment, pivotal trial planning, IND process, and clinical phase plans for RNL, pipeline expansion through additional drug development candidates, and partnership discussions for RNL, DocePLUS and DoxoPLUS; and future development and/or expansion of its product candidates and therapies in its markets. 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 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 in the immediate future; 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
(in thousands, except share and par value data)
|March 31, 2021||December 31,
|Cash and cash equivalents||$||14,447||$||8,346|
|Other current assets||999||829|
|Total current assets||15,446||9,175|
|Property and equipment, net||1,825||1,820|
|Operating lease right-of-use assets||600||636|
|Intangible assets, net||77||86|
|Liabilities and Stockholders’ Equity|
|Accounts payable and accrued expenses||$||1,716||$||2,081|
|Operating lease liability||113||123|
|Term loan obligations, net of discount||6,486||6,335|
|Total current liabilities||8,315||8,539|
|Noncurrent operating lease liability||503||528|
|Preferred stock, $0.001 par value; 5,000,000 shares authorized; 1,952 and 1,954
shares issued and outstanding at March 31, 2021 and December 31, 2020,
|Common stock, $0.001 par value; 100,000,000 shares authorized; 10,180,525
and 6,749,028 shares issued and outstanding at March 31, 2021 and December
31, 2020, respectively
|Additional paid-in capital||445,734||436,535|
|Total stockholders’ equity||9,513||3,031|
|Total liabilities and stockholders’ equity||$||18,336||$||12,105|
|PLUS THERAPEUTICS, INC.
CONSOLIDATED CONDENSED STATEMENTS OF OPERATIONS
(in thousands, except share and per share data)
|For the Three Months Ended March 31,|
|Government contracts and other||$||—||$||118|
|Research and development||1,127||941|
|General and administrative||1,352||1,618|
|Total operating expenses||2,479||2,559|
|Loss from operations||(2,479||)||(2,441||)|
|Other income (expense):|
|Change in fair value of warrants||2||1,667|
|Total other income (expense)||(241||)||1,354|
|Net loss per share, basic and diluted||$||(0.33||)||$||(0.28||)|
|Basic and diluted weighted average shares used in calculating net loss per share
attributable to common stockholders
|PLUS THERAPEUTICS, INC.
CONSOLIDATED CONDENSED STATEMENTS OF CASH FLOWS
|For the Three Months Ended March 31,|
|Cash flows used in operating activities:|
|Adjustments to reconcile net loss to net cash used in operating activities:|
|Depreciation and amortization||88||94|
|Amortization of deferred financing costs and debt discount||151||122|
|Noncash lease expenses||1||4|
|Change in fair value of warrants||(2||)||(1,667||)|
|Share-based compensation expense||107||12|
|Increases (decreases) in cash caused by changes in operating assets and liabilities:|
|Other current assets||(170||)||405|
|Accounts payable and accrued expenses||(461||)||410|
|Net cash used in operating activities||(3,006||)||(1,502||)|
|Cash flows provided by (used in) investing activities:|
|Purchases of property and equipment||(84||)||(11||)|
|Net cash used in investing activities||(84||)||(11||)|
|Cash flows used in financing activities:|
|Payment of financing lease liability||(6||)||(18||)|
|Proceeds from exercise of warrants||2,017||—|
|Proceeds from sale of common stock, net||7,180||—|
|Net cash provided by (used in) financing activities||9,191||(18||)|
|Net increase (decrease) in cash and cash equivalents||6,101||(1,531||)|
|Cash and cash equivalents at beginning of period||8,346||17,592|
|Cash and cash equivalents at end of period||14,447||16,061|
|Supplemental disclosure of cash flows information:|
|Cash paid during period for:|
|Supplemental schedule of non-cash investing and financing activities:|
|Unpaid offering costs||$||102||$||—|