Exhibit 99.1

 

Corbus Pharmaceuticals Reports First Quarter 2023 Financial Results and

Provides Corporate Update

Company expanded precision oncology pipeline with in-licensing of CRB-701: a clinical-stage Nectin-4 antibody drug conjugate (ADC) from CSPC Pharmaceutical Group
CRB-701 Phase 1 dose escalation study ongoing in patients with advanced solid tumors in China
Presented latest CRB-601 anti-αvβ8 mAb pre-clinical data at American Association of Cancer Research (AACR) 2023 annual meeting with IND submission on track for the second half of 2023
Expanded Board of Directors with appointment of Yong Ben, MD

 

Norwood, MA, May 9, 2023 (GLOBE NEWSWIRE) -- Corbus Pharmaceuticals Holdings, Inc. (NASDAQ: CRBP) (“Corbus” or the “Company”), a precision oncology company, today provided a corporate update and reported financial results for the first quarter of 2023.

 

“During our first quarter we continued our evolution into a precision oncology company, led by the execution of our exclusive licensing agreement for CRB-701, a next generation Nectin-4 ADC,” said Yuval Cohen, Ph.D., Chief Executive Officer of Corbus. "We are excited about the potential of this differentiated clinical stage asset that targets Nectin-4 enriched tumors. We also presented additional pre-clinical data at AACR 2023 annual meeting on CRB-601, demonstrating robust target engagement associated with anti-tumor activity alone and in combination with anti-PD-1. We believe this data reinforces the potential of this new approach in blocking activation of TGFβ locally in the TME. We look forward to advancing both CRB-701 and CRB-601 and potentially delivering on a number of milestones in 2023."

 

Key Corporate and Program Updates:

CRB-701 next generation Nectin-4 ADC:
o
Licensed CRB-701 from CSPC Pharmaceutical Group with exclusive development and commercialization rights in the United States, Canada, the European Union (including the European Free Trade Area), the United Kingdom, and Australia.
o
Nectin-4 is a clinically validated tumor associated antigen in urothelial cancer. The Nectin-4 ADC PADCEV® (SeaGen/Astellas) is approved for use in late metastatic urothelial cancer and recently received an expanded label from the Food and Drug Administration based on accelerated approval for use in combination with KEYTRUDA® for patients with locally advanced or metastatic urothelial carcinoma who are ineligible for cisplatin-containing chemotherapy.
o
CRB-701 is designed to achieve an improved therapeutic index and will be explored in urothelial cancer, as well as a range of other Nectin-4 expressing solid tumors.
o
CRB-701 has key features that support a differentiated profile including site-specific conjugation linker chemistry that results in low payload release in plasma and a novel Fc-enabled antibody with an improved pharmacokinetic profile. Pre-clinical data demonstrates the potential to achieve higher exposures with CRB-701 resulting in an improved therapeutic index.

 


 

o
Clinical development is underway and will focus on Nectin-4 positive tumors, including urothelial cancer. CSPC has commenced a Phase 1 dose escalation study in China for patients with advanced solid tumors. Corbus plans to bridge data from this Phase 1 trial to support a U.S. clinical trial starting in mid-2024.
CRB-601 blocking the activation of TGFβ
o
CRB-601 is a potent and selective anti-αvβ8 integrin monoclonal antibody designed to block the activation of latent TGFβ within the tumor micro-environment (TME). CRB-601 significantly inhibits tumor growth as monotherapy and enhances the efficacy of anti-PD-1 immunotherapy as a combination in checkpoint inhibitor (CPI) sensitive and CPI-resistant tumor models.
o
IND submission for CRB-601 is on track for the second half of 2023. The Company expects to enroll the first patient in the Phase 1 study by the end of 2023.
o
Corbus presented pre-clinical data at the AACR 2023 annual meeting indicating that CRB-601 exhibited dose dependent tumor growth inhibition (TGI) in the EMT6 tumor model which was significantly augmented in combination with anti-PD1 therapy. These effects were associated with changes in TME immune cell populations with marked increases in infiltrating T cells, NK cells and M1 polarized macrophages. Efficacy correlated with cell surface αvβ8 occupancy by CRB-601. CRB-601 treatment downregulated phosphorylation of SMAD proteins pSMAD2 and pSMAD3, consistent with blockade of the TGFβ signaling pathway.
o
Corbus hosted the first in the series of virtual “Meet the Expert” events titled “Blocking TGFβ with CRB-601—a New Play for an Old Target,” on April 25th. The event featured Jeffrey Clarke, MD (Duke University School of Medicine) and Joan Seoane, PhD (Vall d'Hebron Institute of Oncology) who discussed the challenges and potential opportunities in targeting Transforming Growth Factor β (TGFβ) in oncology. A replay of the webinar is available from the events page of the Corbus website here.

Addition to the Board:

Dr. Yong Ben joined the Corbus Board of Directors on March 1, 2023. Dr. Ben is an oncology researcher and pharma industry executive, with multiple drug approvals to his credit. He was formerly the Chief Medical Officer of BeiGene, Ltd. and BioAtla, Inc., and led the clinical development of the Immuno-Oncology portfolio for AstraZeneca PLC. This appointment augments our Board with his extensive oncology experience both in the United States and China.

 

Financial Results for Quarter Ended March 31, 2023:

The Company reported a net loss of approximately $17.7 million, or a net loss per diluted share of $4.24, for the three months ended March 31, 2023, compared to a net loss of approximately $9.4 million, or a net loss per diluted share of $2.26, for the same period in 2022.

Operating expenses increased by $8.8 million to approximately $17.3 million for the three months ended March 31, 2023, compared to $8.5 million in the comparable period in the prior year. The increase was primarily attributable to the upfront payment of $7.5 million associated with the CSPC License Agreement, $1.2 million associated with the achievement of a development milestone under the USCF License

 


 

Agreement, and higher drug manufacturing costs offset by reductions in general and administrative expenses associated with legal costs, stock-based compensation expense, and insurance policies.

As of March 31, 2023, the company has $44.2 million of cash and investments on hand which is expected to fund operations through the second quarter of 2024, based on the current planned expenditures.

 

About Corbus

 

Corbus Pharmaceuticals Holdings, Inc. (the “Company” or “Corbus”) is a precision oncology company committed to helping people defeat serious illness by bringing innovative scientific approaches to well understood biological pathways. Corbus’ internal development pipeline includes CRB-701, a next generation antibody drug conjugate (ADC) that targets the expression of Nectin-4 on cancer cells to release a cytotoxic payload and CRB-601, an anti-integrin monoclonal antibody which blocks the activation of TGFβ expressed on cancer cells. Corbus is headquartered in Norwood, Massachusetts. For more information on Corbus, visit corbuspharma.com. Connect with us on Twitter, LinkedIn and Facebook.

Forward-Looking Statements


This press release contains certain forward-looking statements within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934 and Private Securities Litigation Reform Act, as amended, including those relating to the Company's restructuring, trial results, product development, clinical and regulatory timelines, market opportunity, competitive position, possible or assumed future results of operations, business strategies, potential growth opportunities and other statement that are predictive in nature. These forward-looking statements are based on current expectations, estimates, forecasts and projections about the industry and markets in which we operate and management's current beliefs and assumptions.

 

These statements may be identified by the use of forward-looking expressions, including, but not limited to, "expect," "anticipate," "intend," "plan," "believe," "estimate," "potential,” "predict," "project," "should," "would" and similar expressions and the negatives of those terms. These statements relate to future events or our financial performance and involve known and unknown risks, uncertainties, and other factors on our operations, clinical development plans and timelines, which may cause actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements. Such factors include those set forth in the Company's filings with the Securities and Exchange Commission. Prospective investors are cautioned not to place undue reliance on such forward-looking statements, which speak only as of the date of this press release. The Company undertakes no obligation to publicly update any forward-looking statement, whether as a result of new information, future events or otherwise.

 

INVESTOR CONTACT:

Sean Moran

Chief Financial Officer

Corbus Pharmaceuticals

smoran@corbuspharma.com

 

Bruce Mackle
Managing Director
LifeSci Advisors, LLC
bmackle@lifesciadvisors.com

---tables to follow---

 


 

Corbus Pharmaceuticals Holdings, Inc.

Condensed Consolidated Statements of Operations and Comprehensive Loss

(Unaudited)

 

 

For the Three Months
Ended March 31,

 

 

2023

 

 

2022

 

Operating expenses:

 

 

 

 

 

Research and development

 

13,388,343

 

 

 

3,286,236

 

General and administrative

 

3,908,682

 

 

 

5,230,923

 

Total operating expenses

 

17,297,025

 

 

 

8,517,159

 

Operating loss

 

(17,297,025

)

 

 

(8,517,159

)

Other income (expense), net:

 

 

 

 

 

Other income (expense), net

 

229,507

 

 

 

(193,351

)

Interest income (expense), net

 

(678,022

)

 

 

(458,909

)

Foreign currency exchange gain (loss), net

 

728

 

 

 

(267,823

)

Other income (expense), net

 

(447,787

)

 

 

(920,083

)

Net loss

$

(17,744,812

)

 

$

(9,437,242

)

Net loss per share, basic and diluted

$

(4.24

)

 

$

(2.26

)

Weighted average number of common shares outstanding, basic and diluted

 

4,181,556

 

 

 

4,170,043

 

 

 

 

 

 

Comprehensive loss:

 

 

 

 

 

Net loss

$

(17,744,812

)

 

$

(9,437,242

)

Other comprehensive income (loss):

 

 

 

 

 

Change in unrealized gain (loss) on marketable debt securities

 

57,623

 

 

 

(107,248

)

Total other comprehensive income (loss)

 

57,623

 

 

 

(107,248

)

Total comprehensive loss

$

(17,687,189

)

 

$

(9,544,490

)

 

 

 


 

Corbus Pharmaceuticals Holdings, Inc.

Condensed Consolidated Balance Sheets

 

 

 

March 31, 2023

(Unaudited)

 

 

December 31, 2022

 

 

 

 

 

 

 

 

ASSETS

 

 

 

 

 

 

Current assets:

 

 

 

 

 

 

Cash and cash equivalents

 

$

7,324,437

 

 

$

17,002,715

 

Investments

 

 

36,902,563

 

 

 

42,194,296

 

Restricted cash

 

 

192,475

 

 

 

192,475

 

Prepaid expenses and other current assets

 

 

1,445,524

 

 

 

791,616

 

Total current assets

 

 

45,864,999

 

 

 

60,181,102

 

Restricted cash

 

 

477,425

 

 

 

477,425

 

Property and equipment, net

 

 

1,431,945

 

 

 

1,613,815

 

Operating lease right of use assets

 

 

3,688,468

 

 

 

3,884,252

 

Other assets

 

 

182,436

 

 

 

155,346

 

Total assets

 

$

51,645,273

 

 

$

66,311,940

 

LIABILITIES AND STOCKHOLDERS’ EQUITY

 

 

 

 

 

 

Current liabilities:

 

 

 

 

 

 

Notes payable

 

$

203,258

 

 

$

353,323

 

Accounts payable

 

 

1,322,990

 

 

 

2,173,963

 

Accrued expenses

 

 

6,468,302

 

 

 

5,999,252

 

Derivative liability

 

 

36,868

 

 

 

36,868

 

Operating lease liabilities, current

 

 

1,318,671

 

 

 

1,280,863

 

Current portion of long-term debt

 

 

5,008,858

 

 

 

2,795,669

 

Total current liabilities

 

 

14,358,947

 

 

 

12,639,938

 

Long-term debt, net of debt discount

 

 

13,972,360

 

 

 

15,984,426

 

Other long-term liabilities

 

 

2,522,205

 

 

 

22,205

 

Operating lease liabilities, noncurrent

 

 

4,332,809

 

 

 

4,675,354

 

Total liabilities

 

 

35,186,321

 

 

 

33,321,923

 

Stockholders’ equity

 

 

 

 

 

 

Preferred stock, $0.0001 par value; 10,000,000 shares authorized, no shares
   issued and outstanding at March 31, 2023 and December 31, 2022.

 

 

 

 

 

 

Common stock, $0.0001 par value; 300,000,000 shares authorized,
  4,215,133 and 4,171,297 shares issued and outstanding at March 31, 2023 and December 31, 2022, respectively

 

 

422

 

 

 

417

 

Additional paid-in capital

 

 

426,352,478

 

 

 

425,196,359

 

Accumulated deficit

 

 

(409,825,479

)

 

 

(392,080,667

)

Accumulated other comprehensive loss

 

 

(68,469

)

 

 

(126,092

)

Total stockholders’ equity

 

 

16,458,952

 

 

 

32,990,017

 

Total liabilities and stockholders’ equity

 

$

51,645,273

 

 

$

66,311,940