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International Stem Cell Corporation Announces 2021 Fourth Quarter and Year-End Results

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International Stem Cell Corporation (ISCO) announced its 2021 financial results and provided updates on its phase 1 clinical trial for ISC-hpNSC® in treating Parkinson's disease. The company reported a slight revenue increase to $7.18 million, with a notable 127% rise in operating income to $1.35 million. The net loss significantly decreased to $899,000. In clinical outcomes, patients in the trial demonstrated a 47% reduction in % OFF-Time at 12 months and a 43% improvement in quality of life, validating the treatment's safety and efficacy over 48 months.

Positive
  • Revenues slightly increased to $7.18 million from $7.13 million in 2020.
  • Operating income surged 127% to $1.35 million compared to $592,000 in 2020.
  • Net loss decreased by 67% to $899,000 from $2.72 million in 2020.
  • Clinical trial showed a 43% improvement in quality of life for patients after 12 months.
Negative
  • None.

SAN DIEGO, CA / ACCESSWIRE / March 30, 2022 / International Stem Cell Corporation (OTCQX:ISCO) (www.internationalstemcell.com) ("ISCO" or "the Company"), a California-based clinical stage biotechnology company developing novel stem cell-based therapies and biomedical products, today provided a business update and announced fourth quarter and year-end financial results for the period ending on December 31, 2021.

"We are pleased with the outcome of our phase 1 clinical trial as we were able to show not only safety and tolerability, but also preliminary efficacy for ISC-hpNSC®. As an example, on average the quality of life of the patients as measured by the Parkinson's Disease Quality of Life Score-39 Summary Index, improved 43% for the second cohort at twelve months post-transplantation. This improved to a 45% better score in the same at 48 months" stated Andrey Semechkin, Ph.D., CEO and Co-Chairman of ISCO.

FY 2021 Financial Highlights:

  • Revenues slightly increased to $7.18 million in 2021 compared to $7.13 million in 2020.
  • Combined operating income for the year ended December 31, 2021, from our two wholly owned revenue generating subsidiaries, Lifeline Cell Technology and Lifeline Skin Care, increased to $1.35 million, an increase of 127%, compared to $592,000 in 2020.
  • Net loss decreased to $899,000 for the year ended December 31, 2021, a decrease of 67%, compared to $2.72 million in 2020.

Top-line Parkinson's Disease Clinical Trial Results

ISCO successfully completed the treatment phase of its dose escalating phase 1 clinical trial (ClinicalTrials.gov Identifier: NCT02452723) evaluating the safety, tolerability, and preliminary efficacy of its lead candidate, ISC-hpNSC® for the treatment of Parkinson's disease (PD). Patients treated with the mid dose (cohort 2) have been observed for at least 36 months and patients in the low dose group (Cohort 1) have been followed for 48 months post transplantation. In terms of preliminary efficacy, where scores are compared against baseline before transplantation, we observed a potential dose-dependent response, with an apparent peak effectiveness at our middle dose. The % OFF-Time, which is the time during the day when levodopa medication is not performing optimally and PD symptoms return, decreased an average 47% from the baseline at 12 months post transplantation in cohort 2. This trend continued through 24 months where the %OFF time in the second cohort dropped by 55% from the initial reading. The same was true for % ON-Time without dyskinesia, which is the time during the day when levodopa medication is performing optimally without dyskinesia. The % ON-Time increased an average of 42% above the initial evaluation at 12 months post-transplantation in the second cohort. The %ON result improved in the second cohort to 65% above the baseline in month 24. The quality of life of the patients as measured by the Parkinson's Disease Quality of Life Score-39 (PDQ-39) Summary Index, improved 43% for the second cohort at twelve months post-transplantation. This improved to a 45% better score in cohort 2 at 48 months.

About International Stem Cell Corporation

International Stem Cell Corporation is focused on the therapeutic applications of human parthenogenetic stem cells (hpSCs) and the development and commercialization of cell-based research and cosmetic products. ISCO's core technology, parthenogenesis, results in the creation of pluripotent human stem cells from unfertilized oocytes (eggs). hpSCs avoid ethical issues associated with the use or destruction of viable human embryos. ISCO scientists have created the first parthenogenetic, homozygous stem cell line that can be a source of therapeutic cells for hundreds of millions of individuals of differing genders, ages and racial background with minimal immune rejection after transplantation. hpSCs offer the potential to create the first true stem cell bank, UniStemCell™. ISCO also produces and markets specialized cells and growth media for therapeutic research worldwide through its subsidiary Lifeline Cell Technology (www.lifelinecelltech.com), and stem cell-based skin care products through its subsidiary Lifeline Skin Care (www.lifelineskincare.com).

For more information, please visit http://internationalstemcell.com/ or contact: ir@intlstemcell.com

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Safe harbor statement

Statements pertaining to anticipated developments and company achievements, expected clinical studies (including results and ongoing evaluation of the phase 1 clinical trial), and other opportunities for the company and its subsidiaries, along with other statements about the future expectations, beliefs, goals, plans, or prospects expressed by management constitute forward-looking statements. Any statements that are not historical fact (including, but not limited to statements that contain words such as "will," "believes," "plans," "anticipates," "expects," "estimates,") should also be considered to be forward-looking statements. Forward-looking statements involve risks and uncertainties, including, without limitation, risks inherent in the development and/or commercialization of potential products, regulatory approvals, need and ability to obtain capital, application of capital resources among competing uses, and maintenance of intellectual property rights. Actual results may differ materially from the results anticipated in these forward-looking statements and as such should be evaluated together with the many uncertainties that affect the Company's business, particularly those mentioned in the cautionary statements found in the Company's Securities and Exchange Commission filings. The Company disclaims any intent or obligation to update forward-looking statements.

International Stem Cell Corporation and Subsidiaries
Consolidated Balance Sheets
(In thousands, except share and par value data)


December 31, December 31,
2021 2020
Assets


Current assets:


Cash
$171 $689
Accounts receivable, net
844 403
Inventory, net
1,184 917
Prepaid expenses and other current assets
135 174
Total current assets
2,334 2,183
Non-current inventory, net
372 371
Property and equipment, net
384 534
Intangible assets, net
949 1,262
Right-of-use assets
868 874
Deposits and other assets
39 63
Total assets
$4,946 $5,287
Liabilities, Redeemable Convertible Preferred Stock and Stockholders' Deficit
Current liabilities:
Accounts payable
$508 $360
Accrued liabilities
404 386
Operating lease liabilities, current
179 346
Advances
250 250
Related party note payable
2,943 -
Paycheck Protection Program loan, current
- 141
Total current liabilities
4,284 1,483
Related party note payable
- 2,475
Paycheck Protection Program loan, net of current portion
- 517
Operating lease liabilities, net of current portion
950 845
Total liabilities
5,234 5,320
Commitments and contingencies (Note 11)
Series D redeemable convertible preferred stock, $0.001 par value; 50 shares
authorized; 43 shares issued and outstanding; liquidation preference of $4,300
at December 31, 2021 and 2020
4,300 4,300
Stockholders' Deficit:
Non-redeemable convertible preferred stock, $0.001 par value; 10,004,310 and 10,006,310
shares authorized, 5,254,310 and 5,255,124 shares issued and outstanding, liquidation
preference of $9,766 and $10,565 at December 31, 2021 and December 31, 2020,
respectively
5 5
Common stock, $0.001 par value; 120,000,000 shares authorized; 8,004,389 and 7,539,089
shares issued and outstanding at December 30, 2021 and 2020, respectively
8 8
Additional paid-in capital
105,413 104,769
Accumulated deficit
(110,014) (109,115)
Total stockholders' deficit
(4,588) (4,333)
Total liabilities, redeemable convertible preferred stock
and stockholders' deficit
$4,946 $5,287

International Stem Cell Corporation and Subsidiaries
Consolidated Statements of Operations
(In thousands, except per share data)


Years Ended December 31,
2021 2020
Product sales
$7,176 $7,128
Operating expenses:
Cost of sales
2,935 2,781
General and administrative
4,084 4,422
Selling and marketing
1,383 1,755
Research and development
695 988
Total operating expenses
9,097 9,946
Loss from operations
(1,921) (2,818)
Other income (expense):
Gain on forgiveness of debt
1,137 -
Change in fair value of warrant liability
- 207
Interest expense
(128) (113)
Other income, net
13 -
Total other income, net
1,022 94
Net loss
$(899) $(2,724)
Net loss per common share, basic and diluted
$(0.11) $(0.36)
Weighted-average common shares used to compute
net loss per share, basic and diluted
7,833 7,539

Contacts:
International Stem Cell Corporation
Russell A. Kern, PhD
Phone: 760-940-6383
Email: ir@intlstemcell.com

SOURCE: International Stem Cell CORP



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FAQ

What were the financial results of ISCO for 2021?

International Stem Cell Corporation reported revenues of $7.18 million, operating income of $1.35 million, and a net loss of $899,000 in 2021.

What clinical trial results did ISCO announce?

ISCO announced a 43% improvement in quality of life for patients treated with ISC-hpNSC® after 12 months, along with significant reductions in % OFF-Time.

What is the significance of the phase 1 clinical trial results for ISCO?

The phase 1 clinical trial for ISC-hpNSC® indicated safety, tolerability, and preliminary efficacy, making a case for further development in Parkinson's disease treatment.

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