STOCK TITAN

Pyxis Oncology (NASDAQ: PYXS) widens Q2 loss while bolstering cash runway

(Moderate)
(Neutral)
Form Type
8-K

Rhea-AI Filing Summary

Pyxis Oncology, Inc. reported second quarter 2026 results and detailed progress for its lead antibody-drug conjugate, micvotabart pelidotin (MICVO), in recurrent/metastatic head and neck squamous cell carcinoma. For the quarter ended June 30, 2026, the company recorded a net loss of $25.3 million, or ($0.40) per share, compared with a net loss of $18.4 million, or ($0.30) per share, a year earlier, driven mainly by higher general and administrative expenses.

Research and development expenses were $16.1 million versus $17.1 million in the prior-year quarter, while general and administrative expenses increased to $9.9 million from $5.4 million, largely due to severance and stock-based compensation. As of June 30, 2026, cash, cash equivalents, restricted cash and short-term investments totaled $34.5 million.

The company completed a private placement of up to $114 million, providing approximately $50 million in upfront gross proceeds (of which $10.0 million was received by June 30, 2026) and extending its cash runway into the second quarter of 2027. Updated MICVO monotherapy data in 2L+ R/M HNSCC are expected in Fall 2026, with updated first-line combination data with KEYTRUDA in the fourth quarter of 2026. MICVO holds U.S. FDA Fast Track Designation in R/M HNSCC.

Positive

  • Completed a private placement of up to $114 million, including approximately $50 million in upfront gross proceeds to support MICVO clinical development.
  • Cash, cash equivalents, restricted cash and short-term investments plus upfront financing are expected to fund operations into the second quarter of 2027, providing visibility on near-term liquidity.
  • Lead asset MICVO has Fast Track Designation from the U.S. FDA for R/M HNSCC after platinum and anti-PD-(L)1 therapy, underscoring regulatory support for the program.
  • Key MICVO readouts are planned, with updated Phase 1 monotherapy data in Fall 2026 and Phase 1/2 combination data in Q4 2026, which may further clarify clinical potential.

Negative

  • Quarterly net loss increased to $25.3 million from $18.4 million year over year, reflecting higher operating expenses.
  • Milestone revenue fell to $0 in the quarter from $2.8 million in the prior-year quarter, removing a prior revenue contribution.
  • General and administrative expenses rose to $9.9 million from $5.4 million, driven by severance and stock-based compensation, pressuring the cost structure.
  • Total assets declined to $54.9 million at June 30, 2026 from $91.5 million at year-end 2025, and stockholders’ equity decreased to $11.4 million from $53.4 million.
Item 2.02 Results of Operations and Financial Condition Financial
Disclosure of earnings results, typically an earnings press release or preliminary financials.
Item 9.01 Financial Statements and Exhibits Exhibits
Financial statements, pro forma financial information, and exhibit attachments filed with this report.
Net loss Q2 2026 $25.3 million Net loss for the quarter ended June 30, 2026
Net loss per share Q2 2026 $0.40 Basic and diluted net loss per common share for Q2 2026
Cash and investments $34.5 million Cash, cash equivalents, restricted cash and short-term investments as of June 30, 2026
Private placement size $114 million Total potential proceeds from June–July 2026 private placement financing
Upfront private placement proceeds $50 million Approximate upfront gross proceeds from private placement completed July 2, 2026
R&D expense Q2 2026 $16.1 million Research and development expenses for the quarter ended June 30, 2026
G&A expense Q2 2026 $9.9 million General and administrative expenses for the quarter ended June 30, 2026
Shares outstanding 83,408,050 Common shares outstanding as of August 12, 2026
antibody-drug conjugate medical
"The Company’s lead candidate, micvotabart pelidotin (MICVO), is a first-in-concept antibody-drug conjugate (ADC)"
An antibody-drug conjugate is a targeted medicine that combines an antibody, which can identify specific cells, with a powerful drug designed to destroy those cells. This approach allows for precise treatment, minimizing damage to healthy tissue. For investors, developments in this area can signal advances in cancer therapies and potential growth opportunities in the biotech sector.
Fast Track Designation regulatory
"MICVO received Fast Track Designation from the U.S. Food and Drug Administration"
Fast track designation is a status the U.S. Food and Drug Administration grants to drugs intended to treat serious conditions and address an unmet medical need. It gives the developer more frequent communication with the FDA and can allow parts of the application to be reviewed on a rolling basis, and it may pave the way to priority review or accelerated approval. It can shorten development timelines, though it does not guarantee approval.
dose expansion study medical
"Part 2, a dose expansion study in 2L+ R/M HNSCC, is currently ongoing"
private placement financing financial
"Pyxis Oncology announced up to $114 million of private placement financing with new and existing investors"
Private placement financing is when a company raises money by selling stocks, bonds or other securities directly to a small group of chosen investors instead of offering them on the public market. For investors it matters because these deals can change ownership stakes, bring fresh cash for growth or debt reduction, and affect how easy it is to buy or sell those securities later—think of it like inviting a few private backers into a business rather than opening the door to the whole neighborhood.
sublease income financial
"Sublease income 389 684 1,020 1,199"
operating lease right-of-use asset financial
"Operating lease right-of-use asset 10,951 11,418"
An operating lease right-of-use asset is the accounting entry that shows a company’s recorded value of its legal right to use leased property or equipment for a set period, similar to listing the worth of a long-term rental agreement on the balance sheet. It matters to investors because it makes leased obligations and the economic benefit of rented assets visible, affecting reported assets, leverage and how future lease costs are reflected in financial statements — like seeing both a rented shop’s utility and the remaining rent commitment.
Milestone revenue $0 Down from $2.8 million in the quarter ended June 30, 2025
Net loss $25.3 million Worse than $18.4 million in the quarter ended June 30, 2025
R&D expense $16.1 million Slightly lower than $17.1 million in the quarter ended June 30, 2025
G&A expense $9.9 million Higher than $5.4 million in the quarter ended June 30, 2025

FAQ

What were Pyxis Oncology (PYXS) key financial results for Q2 2026?

Pyxis Oncology reported a net loss of $25.3 million, or ($0.40) per share, for the quarter ended June 30, 2026, versus a net loss of $18.4 million, or ($0.30) per share, in the same 2025 quarter.

How much cash does Pyxis Oncology (PYXS) have and how long is its runway?

As of June 30, 2026, Pyxis Oncology held $34.5 million in cash, cash equivalents, restricted cash and short-term investments. Together with $50 million upfront financing, this is expected to fund operations into the second quarter of 2027.

What are the details of Pyxis Oncology (PYXS) private placement financing?

In June 2026, Pyxis Oncology arranged a private placement for up to $114 million. The transaction provided approximately $50 million in upfront gross proceeds, with up to about $64 million more possible if accompanying warrants are fully exercised for cash.

How did Pyxis Oncology (PYXS) R&D and G&A expenses change in Q2 2026?

Research and development expenses were $16.1 million in Q2 2026 versus $17.1 million a year earlier. General and administrative expenses increased to $9.9 million from $5.4 million, primarily due to severance and higher stock-based compensation.

What clinical milestones are upcoming for MICVO at Pyxis Oncology (PYXS)?

Pyxis Oncology expects updated Phase 1 monotherapy data in Fall 2026 for 2L+ R/M HNSCC and Phase 1/2 combination data in Q4 2026 for first-line R/M HNSCC patients treated with MICVO plus KEYTRUDA.

What regulatory status does MICVO have at Pyxis Oncology (PYXS)?

MICVO, Pyxis Oncology’s lead ADC, has Fast Track Designation from the U.S. FDA for adults with recurrent/metastatic HNSCC whose disease progressed after platinum-based chemotherapy and anti-PD-(L)1 therapy, supporting expedited development.

How many Pyxis Oncology (PYXS) shares are outstanding?

As of August 12, 2026, Pyxis Oncology had 83,408,050 shares of common stock outstanding. This figure reflects the company’s equity base following its recent operating and financing activities.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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0001782223false00017822232026-08-132026-08-13

 

UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549

 

FORM 8-K

 

CURRENT REPORT

Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934

Date of Report (Date of earliest event reported): August 13, 2026

 

 

Pyxis Oncology, Inc.

(Exact name of Registrant as Specified in Its Charter)

 

 

Delaware

001-40881

83-1160910

(State or Other Jurisdiction
of Incorporation)

(Commission File Number)

(IRS Employer
Identification No.)

 

 

 

 

 

321 Harrison Avenue

 

Boston, Massachusetts

 

02118

(Address of Principal Executive Offices)

 

(Zip Code)

 

Registrant’s Telephone Number, Including Area Code: (617) 453-3596

 

(Former Name or Former Address, if Changed Since Last Report)

 

Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:

Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)
Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))
Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))

Securities registered pursuant to Section 12(b) of the Act:


Title of each class

 

Trading
Symbol(s)

 


Name of each exchange on which registered

Common Stock, par value $0.001 per share

 

PYXS

 

The Nasdaq Global Select Market

Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§ 230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§ 240.12b-2 of this chapter).

Emerging growth company

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act.

 


Item 2.02 Results of Operations and Financial Condition.

On August 13, 2026, Pyxis Oncology, Inc. (“the Company”) issued a press release announcing its financial results for the quarter ended June 30, 2026 and provided a corporate update. A copy of the press release is furnished as Exhibit 99.1 to this Current Report on Form 8-K and is incorporated herein by reference.

 

The information contained in Item 2.02 of this Current Report, including Exhibit 99.1, shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended, or otherwise subject to the liabilities of that section, nor shall it be deemed incorporated by reference into any other filing with the U.S. Securities and Exchange Commission made by the Company, regardless of any general incorporation language in such filings.


Item 9.01 Financial Statements and Exhibits.

(d) Exhibits

Exhibit No.

Description

99.1

Press Release dated August 13, 2026

104

Cover Page Interactive Data File (embedded within the Inline XBRL document)

 

 


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.

 

 

 

Pyxis Oncology, Inc.

 

 

 

 

Date:

August 13, 2026

By:

/s/ Jitendra Wadhane

 

 

 

Jitendra Wadhane
Principal Financial and Accounting Officer
 

 


img244827169_0.jpg

Exhibit 99.1

 

Pyxis Oncology Reports Second Quarter 2026 Financial Results and Advances MICVO Toward Key 2026 Clinical Milestones

 

Updated data from the MICVO Phase 1 monotherapy study in 2L+ R/M HNSCC on track to be reported in Fall 2026; update to include detailed analyses of patients treated at or below a dose cap

 

Updated data from the MICVO Phase 1/2 combination study with pembrolizumab in 1L R/M HNSCC on track to be reported in the fourth quarter of 2026

 

Completed private placement financing for up to $114 million, providing approximately $50 million in upfront gross proceeds to support additional patient follow-up

 

Upfront proceeds from the private placement, together with existing cash, extended the Company’s cash runway into the second quarter of 2027

 

BOSTON, August 13, 2026 (GLOBE NEWSWIRE)— Pyxis Oncology, Inc. (Nasdaq: PYXS), a clinical-stage company developing next-generation therapeutics for difficult-to-treat cancers, today reported financial results for the quarter ended June 30, 2026, and highlighted continued advancement of the micvotabart pelidotin (MICVO) clinical development programs.

 

“The second quarter was marked by continued execution across the MICVO program and a financing that strengthened our balance sheet and extended our cash runway into the second quarter of 2027,” said Tom Civik, Interim Chief Executive Officer and Director of Pyxis Oncology. “The additional capital gives us greater flexibility to incorporate longer patient follow-up and planned analyses into our next clinical updates. We expect to report updated monotherapy data in second-line and beyond recurrent/metastatic head and neck squamous cell carcinoma (2L+ R/M HNSCC) this fall, followed by updated first-line combination data with pembrolizumab in the fourth quarter. We remain focused on generating the clinical evidence needed to evaluate MICVO’s potential to address the significant unmet need in head and neck cancer, regardless of HPV status or prior therapy.”

 

Pipeline & Corporate Updates

Pyxis Oncology expects to report updated data from the ongoing MICVO Phase 1 monotherapy study for 2L+ R/M HNSCC in Fall 2026. The update is expected to include patients treated at 5.4 mg/kg IV Q3W with a dose equivalent to or below a dose cap, together with detailed analyses of the dose cap impact on safety, tolerability, efficacy and initial durability.
The Company completed target enrollment in the Phase 1 Part 2 monotherapy dose expansion study in the first quarter of 2026.
The ongoing MICVO Phase 1 monotherapy study is a multi-part study. Part 1 was a dose escalation study across multiple doses and tumor types, with initial results shared in November 2024. Part 2, a dose expansion study in 2L+ R/M HNSCC, is currently ongoing. Preliminary Phase 1 study results in 2L+ R/M HNSCC were shared in December 2025, supporting MICVO’s broad potential to address a significant unmet need for patients regardless of HPV status or prior therapy.
The dose expansion study of the ongoing MICVO Phase 1 monotherapy study includes two arms: post-platinum and anti-PD-(L)1-experienced patients (Arm 1) and post-EGFRi and anti-PD-(L)1-experienced patients (Arm 2). Target enrollment for each arm of the study was n=~20.
In December 2025, a dose cap was implemented for higher body weight patients. Based on internal PK simulation modeling indicating that MICVO exposures with dose capping and adjusted ideal bodyweight (AIBW) dosing are expected to be comparable, dose capping was prioritized due to its operational simplicity and speed of implementation. The Fall 2026 monotherapy disclosure will remain focused on patients treated at or below the dose cap.
Pyxis Oncology expects to report updated data from the ongoing Phase 1/2 combination dose escalation study of MICVO and Merck’s (known as MSD outside of the US and Canada) anti-PD-1 therapy KEYTRUDA® (pembrolizumab) for 1L R/M HNSCC patients in the fourth quarter of 2026.

 

 


img244827169_0.jpg

The ongoing MICVO Phase 1/2 study evaluating MICVO in combination with KEYTRUDA® (pembrolizumab) is currently in dose escalation across multiple doses for the treatment of 1L R/M HNSCC. Preliminary positive results for the treatment of 1L/2L+ R/M HNSCC were shared in December 2025.
In June 2026, Pyxis Oncology announced up to $114 million of private placement financing with new and existing healthcare-focused investors to advance MICVO through key clinical milestones.
On July 2, 2026, the Company completed the private placement which resulted in upfront gross proceeds of approximately $50 million, before deducting placement agent fees and offering expenses, and anticipates up to an additional approximately $64 million of gross proceeds, before placement agent fees, if the accompanying warrants are exercised in full for cash.
The upfront proceeds from the private placement, together with existing cash, extended the Company’s cash runway into the second quarter of 2027. The additional capital from the private placement provides flexibility to continue patient follow-up and allow the data to mature following completion of enrollment of the 2L+ R/M HNSCC study.

 

Second Quarter 2026 Financial Results

As of June 30, 2026, Pyxis Oncology had cash and cash equivalents, including restricted cash, and short-term investments, of $34.5 million. Additionally, on July 2, 2026, the Company completed the private placement which resulted in upfront gross proceeds of approximately $50 million (of which $10.0 million was received on June 30, 2026), before deducting placement agent fees and offering expenses. The Company believes that its cash and cash equivalents, including restricted cash, and short-term investments as of June 30, 2026, along with the upfront proceeds from the private placement, will be sufficient to fund its operations into the second quarter of 2027.
Research and development expenses were $16.1 million for the quarter ended June 30, 2026, compared to $17.1 million for the quarter ended June 30, 2025. The decrease was primarily due to a $3.5 million increase in clinical trial related expenses related to monotherapy and combination therapy of MICVO, $1.1 million increase in preclinical studies, offset by a reduction of $4.7 million in manufacturing costs.
General and administrative expenses were $9.9 million for the quarter ended June 30, 2026, compared to $5.4 million for the quarter ended June 30, 2025. The increase was primarily due to an increase in severance costs and higher stock-based compensation.
Net loss was $25.3 million, or ($0.40) per common share, for the quarter ended June 30, 2026, compared to $18.4 million, or ($0.30) per common share, for the quarter ended June 30, 2025. Excluding non-cash stock-based compensation expense, the net loss for the quarter ended June 30, 2026 was $19.8 million, compared to a net loss of $15.3 million for the quarter ended June 30, 2025.
As of August 12, 2026, the outstanding number of shares of Common Stock of Pyxis Oncology was 83,408,050.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 


img244827169_0.jpg

About Pyxis Oncology, Inc.

Pyxis Oncology, Inc. is a clinical-stage biopharmaceutical company developing therapeutics for difficult-to-treat cancers. The Company’s lead candidate, micvotabart pelidotin (MICVO), is a first-in-concept antibody-drug conjugate (ADC) that targets extradomain-B of fibronectin (EDB+FN), a non-cellular structural component of the tumor extracellular matrix (ECM). EDB+FN is selectively overexpressed in the tumor microenvironment of a wide range of solid tumors and largely absent from normal adult tissues. MICVO is designed to treat solid tumors through a three-pronged mechanism of action: direct cancer cell killing, bystander effect and immunogenic cell death. MICVO is currently being evaluated as monotherapy in a Phase 1 clinical study in patients with recurrent and metastatic head and neck squamous cell carcinoma (R/M HNSCC) and in combination with Merck’s anti-PD-1 therapy, KEYTRUDA® (pembrolizumab) in a Phase 1/2 clinical study in patients with R/M HNSCC and other solid tumors. Pyxis Oncology is focused on advancing MICVO, with the goal of improving outcomes for patients living with R/M HNSCC and contributing to meaningful progress in cancer treatment.

 

MICVO received Fast Track Designation from the U.S. Food and Drug Administration for the treatment of adult patients with R/M HNSCC whose disease has progressed following treatment with platinum-based chemotherapy and an anti-PD-(L)1 therapy.

 

KEYTRUDA® is a registered trademark of Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA.

 

To learn more, visit www.pyxisoncology.com or follow us on LinkedIn.

 

Forward Looking Statements

This press release contains forward-looking statements for the purposes of the safe harbor provisions under the Private Securities Litigation Reform Act of 1995 and other federal securities laws. These statements are often identified by the use of words such as “anticipate,” “believe,” “can,” “continue,” “could,” “estimate,” “expect,” “intend,” “likely,” “may,” “might,” “objective,” “ongoing,” “plan,” “potential,” “predict,” “project,” “should,” “to be,” “will,” “would,” or the negative or plural of these words, or similar expressions or variations, although not all forward-looking statements contain these words. We cannot assure you that the events and circumstances reflected in the forward-looking statements will be achieved or occur and actual results could differ materially from those expressed or implied by these forward-looking statements. Factors that could cause or contribute to such differences include, but are not limited to, those identified herein, and those discussed in the section titled “Risk Factors” set forth in Part II, Item 1A. of the Company’s Quarterly Report on Form 10-Q filed with the SEC on August 13, 2026, and our other filings, each of which is on file with the Securities and Exchange Commission. These risks are not exhaustive. New risk factors emerge from time to time, and it is not possible for our management to predict all risk factors, nor can we assess the impact of all factors on our business or the extent to which any factor, or combination of factors, may cause actual results to differ materially from those contained in any forward-looking statements. In addition, statements that “we believe” and similar statements reflect our beliefs and opinions on the relevant subject. These statements are based upon information available to us as of the date hereof and while we believe such information forms a reasonable basis for such statements, such information may be limited or incomplete, and our statements should not be read to indicate that we have conducted an exhaustive inquiry into, or review of, all potentially available relevant information. These statements are inherently uncertain, and investors are cautioned not to unduly rely upon these statements. Except as required by law, we undertake no obligation to update any forward-looking statements to reflect events or circumstances after the date of such statements.

 

Pyxis Oncology Contact

IR@pyxisoncology.com

 


img244827169_0.jpg

PYXIS ONCOLOGY, INC.

Condensed Consolidated Statements of Operations and Comprehensive Loss

(In thousands, except share and per share amounts)

(Unaudited)

 

Three Months Ended June 30,

 

 

Six Months Ended June 30,

 

 

2026

 

 

2025

 

 

2026

 

 

2025

 

Milestone revenue

 

$

 

 

$

2,820

 

 

$

 

 

$

2,820

 

Operating expenses:

 

 

 

 

 

 

 

 

 

 

 

 

Research and development

 

 

16,057

 

 

 

17,133

 

 

 

36,040

 

 

 

34,177

 

General and administrative

 

 

9,933

 

 

 

5,437

 

 

 

14,310

 

 

 

11,307

 

Total operating expenses

 

 

25,990

 

 

 

22,570

 

 

 

50,350

 

 

 

45,484

 

Loss from operations

 

 

(25,990

)

 

 

(19,750

)

 

 

(50,350

)

 

 

(42,664

)

Other income, net:

 

 

 

 

 

 

 

 

 

 

 

 

Interest and investment income, net

 

 

255

 

 

 

995

 

 

 

712

 

 

 

2,236

 

Sublease income

 

 

389

 

 

 

684

 

 

 

1,020

 

 

 

1,199

 

Total other income, net

 

 

644

 

 

 

1,679

 

 

 

1,732

 

 

 

3,435

 

Loss before income taxes

 

 

(25,346

)

 

 

(18,071

)

 

 

(48,618

)

 

 

(39,229

)

Income tax expense

 

 

 

 

 

283

 

 

 

 

 

 

283

 

Net loss

 

$

(25,346

)

 

$

(18,354

)

 

$

(48,618

)

 

$

(39,512

)

Net loss per common share - basic and diluted

 

$

(0.40

)

 

$

(0.30

)

 

$

(0.76

)

 

$

(0.64

)

Weighted average shares of common stock outstanding - basic and diluted

 

 

63,991,609

 

 

 

61,918,826

 

 

 

63,695,177

 

 

 

61,486,290

 

Other comprehensive loss:

 

 

 

 

 

 

 

 

 

 

 

 

Net unrealized loss on marketable debt securities

 

 

(4

)

 

 

(54

)

 

 

(57

)

 

 

(175

)

Other comprehensive loss

 

 

(4

)

 

 

(54

)

 

 

(57

)

 

 

(175

)

Comprehensive loss

 

$

(25,350

)

 

$

(18,408

)

 

$

(48,675

)

 

$

(39,687

)

 


 

 

 

 

 

 

 

 

 

 

 

 

 


img244827169_0.jpg

PYXIS ONCOLOGY, INC.

Condensed Consolidated Balance Sheets

(In thousands, except share and per share amounts)

(Unaudited)

 

 

June 30, 2026

 

 

December 31, 2025

 

Assets

 

 

 

 

 

 

Current assets:

 

 

 

 

 

 

Cash and cash equivalents

 

$

18,855

 

 

$

15,422

 

Marketable debt securities

 

 

14,141

 

 

 

51,435

 

Restricted cash

 

 

1,472

 

 

 

1,472

 

Prepaid expenses and other current assets

 

 

2,266

 

 

 

3,776

 

Total current assets

 

 

36,734

 

 

 

72,105

 

Property and equipment, net

 

 

7,237

 

 

 

7,997

 

Operating lease right-of-use asset

 

 

10,951

 

 

 

11,418

 

Total assets

 

$

54,922

 

 

$

91,520

 

Liabilities and Stockholders’ Equity

 

 

 

 

 

 

Current liabilities:

 

 

 

 

 

 

Accounts payable

 

$

3,269

 

 

$

10,885

 

Private placement advance liability

 

 

10,000

 

 

 

 

Accrued expenses and other current liabilities

 

 

12,381

 

 

 

8,554

 

Operating lease liabilities, current portion

 

 

1,824

 

 

 

1,692

 

Total current liabilities

 

 

27,474

 

 

 

21,131

 

Operating lease liabilities, net of current portion

 

 

16,008

 

 

 

16,958

 

Financing lease liabilities, net of current portion

 

 

 

 

 

23

 

Total liabilities

 

 

43,482

 

 

 

38,112

 

Commitments and contingencies

 

 

 

 

 

 

Stockholders’ equity:

 

 

 

 

 

 

Preferred stock

 

 

 

 

 

 

Common stock

 

 

63

 

 

 

63

 

Additional paid-in capital

 

 

503,176

 

 

 

496,469

 

Accumulated other comprehensive (loss) income

 

 

(4

)

 

 

53

 

Accumulated deficit

 

 

(491,795

)

 

 

(443,177

)

Total stockholders’ equity

 

 

11,440

 

 

 

53,408

 

Total liabilities and stockholders’ equity

 

$

54,922

 

 

$

91,520

 

 

 

 

 

 

 

 

 


Filing Exhibits & Attachments

2 documents