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GW Pharmaceuticals plc Reports Second Quarter 2020 Financial Results and Operational Progress

- Total revenue increased 68 percent to $121.3 million -
- Epidiolex approved in the U.S. for seizures associated with TSC, launch expected this month -
- Conference call today at 4:30 p.m. EDT –

LONDON and CARLSBAD, Calif., Aug. 06, 2020 (GLOBE NEWSWIRE) -- GW Pharmaceuticals plc (Nasdaq: GWPH), a world leader in the science, development, and commercialization of cannabinoid prescription medicines, today announced financial results and operating progress for the second quarter ended June 30, 2020.

“We were pleased with the strength of U.S. Epidiolex sales in the second quarter in spite of the COVID-19 pandemic. Further, the recent approval and imminent launch of Epidiolex for the treatment of seizures associated with TSC provides a meaningful new opportunity to accelerate momentum through the second half of 2020 and beyond,” stated Justin Gover, GW’s CEO. “We also continue to be excited about the potential of our product pipeline, in particular nabiximols, for which we recently outlined our accelerated US development strategy in the treatment of spasticity in patients with MS and other conditions. We look forward to commencing the nabiximols Phase 3 program as well as multiple other pipeline clinical trials in the second half of the year.”

FINANCIAL RESULTS

  • Total revenue for the quarter ended June 30, 2020 was $121.3 million compared to $72.0 million for the quarter ended June 30, 2019

  • Net loss for the quarter ended June 30, 2020 was $8.8 million compared to net income of $79.7 million for the quarter ended June 30, 2019. The prior year quarter included net proceeds of $104.1 million from the sale of a Rare Pediatric Priority Review Voucher.

  • Cash and cash equivalents at June 30, 2020 were $477.6 million

OPERATIONAL HIGHLIGHTS

  • Epidiolex (cannabidiol) progress:

    • Total Q2 net product sales of Epidiolex of $117.7 million

    • U.S. commercial update

      • U.S. Epidiolex Q2 net product sales of $111.1 million

      • TSC indication approved by FDA, August commercial launch planned

      • TSC payer reimbursement anticipated quickly following launch

    • European commercial update

      • Ex-U.S. Epidyolex Q2 net product sales of $6.6 million

      • Pricing & reimbursement progress in Germany, France and Italy

      • TSC EMA submission under review

    • Clinical progress with additional indications

      • Phase 3 trial in Rett Syndrome expected to re-commence in H2 2020

    • Strengthening commercial exclusivity

      • Orphan exclusivity in both the U.S. and EU

      • 3 new patents granted and listed in Orange Book, bringing total of 13 patents listed in Orange Book, 12 of which expire in 2035

        • One recent patent listed is a non-use patent directed to the oral formulation

      • Epidiolex composition patent application in process

      • TSC patent applications under review

  • Nabiximols

    • MS Spasticity Clinical program

      • Three positive Phase 3 MS spasticity trials already completed outside of the U.S.

      • Five new MS Spasticity Phase 3 trials expected to commence in H2 2020 (2) and H1 2021 (3), any one of which could enable a NDA submission

        • Phase 3 muscle tone studies – placebo-controlled cross-over design

          • N=52; Expected start: Q4 2020

          • N=190; Expected start: Q1 2021

          • N=36 (nabiximols responders); Expected start: Q1 2021

        • Phase 3 spasm frequency studies – placebo-controlled parallel group

          • N=450; Expected start: Q4 2020

          • N=~200 (nabiximols responders); Expected start: Q2 2021

    • Spinal Cord Injury (SCI) spasticity clinical program

      • Three SCI trials expected to be initiated in 2020 and 2021

      • N=~100 (observational clinical discovery study); Expected start: Q4 2020

      • N=~100 (muscle tone in nabiximols responders); Placebo-controlled parallel group design. Expected start: Q2 2021

      • N=~400 (spasm frequency); Placebo-controlled parallel group design. Expected start: H2 2021

    • Post-Traumatic Stress Disorder (PTSD) clinical program

      • Phase 2/3 study in PTSD (N=~ 325); Expected start: H1 2021

  • Additional pipeline programs

    • Schizophrenia (GWP42003)

      • Phase 2b trial expected to commence H2 2020

    • CBDV in autism trials expected to recommence in H2 2020

      • 30-patient open label study in autism

      • Investigator-led 100 patient placebo-controlled trial in autism

    • Neonatal Hypoxic-Ischemic Encephalopathy (NHIE) intravenous CBD program

      • Phase 1b safety study in patients continues to recruit

      • Orphan Drug and Fast Track Designations granted from FDA and EMA

Conference Call and Webcast Information

GW Pharmaceuticals will host a conference call and webcast today at 4:30 pm EDT. To participate in the conference call, please dial 833-937-1050 (toll free from the U.S. and Canada) or 845-403-8302 (international). Investors may also access a live audio webcast of the call via the investor relations section of the Company’s website at http://www.gwpharm.com. A replay of the call will also be available through the GW website shortly after the call and will remain available for 90 days. Replay Numbers: (toll free):1-877-481-4010 or 919-882-2331 (international). For both dial-in numbers please use conference Replay ID: 35770.

About GW Pharmaceuticals plc and Greenwich Biosciences, Inc.

Founded in 1998, GW is a biopharmaceutical company focused on discovering, developing and commercializing novel therapeutics from its proprietary cannabinoid product platform in a broad range of disease areas. The Company’s lead product, EPIDIOLEX® (cannabidiol) oral solution, is commercialized in the U.S. by its U.S. subsidiary Greenwich Biosciences for the treatment of seizures associated with Lennox-Gastaut syndrome (LGS), Dravet syndrome, or tuberous sclerosis complex (TSC) in patients one year of age and older. This product has received approval in the European Union under the tradename EPIDYOLEX® for the adjunctive treatment of seizures associated with LGS or Dravet syndrome in conjunction with clobazam in patients two years and older and is under EMA review for the treatment of TSC. GW is currently carrying out a Phase 3 trial in Rett syndrome. The Company has a deep pipeline of additional cannabinoid product candidates, in particular nabiximols, for which the Company is advancing multiple late-stage clinical programs in order to seek FDA approval in the treatment of spasticity associated with multiple sclerosis and spinal cord injury, as well as for the treatment of PTSD. The Company has additional cannabinoid product candidates in Phase 2 trials for autism and schizophrenia. For further information, please visit www.gwpharm.com.

Forward-looking statements
This news release contains forward-looking statements that reflect GW's current expectations regarding future events, including statements regarding financial performance, the timing of clinical trials, the timing and outcomes of regulatory or intellectual property decisions, the relevance of GW products commercially available and in development, the clinical benefits of EPIDIOLEX®/EPIDYOLEX® (cannabidiol) oral solution and Sativex® (nabiximols), and the safety profile and commercial potential of both medicines, and those associated with the COVID-19 pandemic. Forward-looking statements involve risks and uncertainties. Actual events could differ materially from those projected herein and depend on a number of factors, including (inter alia), the success of GW’s research strategies, the applicability of the discoveries made therein, the successful and timely completion and uncertainties related to the regulatory process, and the acceptance of EPIDIOLEX®/EPIDYOLEX®, Sativex® and other products by consumer and medical professionals. A further list and description of risks and uncertainties associated with an investment in GW can be found in GW’s filings with the U.S. Securities and Exchange Commission. Existing and prospective investors are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date hereof. GW undertakes no obligation to update or revise the information contained in this press release, whether as a result of new information, future events or circumstances or otherwise.

Enquiries:

GW Pharmaceuticals plc

Stephen Schultz, VP Investor Relations

917 280 2424 / 401 500 6570

U.S. Media Enquiries:
Sam Brown Inc. Healthcare Communications

Christy Curran
Mike Beyer

615 414 8668
312 961 2502

Ex-U.S. media enquiries

Ben Atwell, FTI Consulting

+44 (0)203 727 1000


GW PHARMACEUTICALS PLC
CONDENSED CONSOLIDATED BALANCE SHEETS
(in thousands, except share data)
(unaudited)

June 30,

December 31,

2020

2019

Assets

Cash and cash equivalents

$

477,557

$

536,933

Accounts receivable, net

80,357

48,883

Inventory

99,620

85,528

Prepaid expenses and other current assets

30,183

28,292

Total current assets

687,717

699,636

Property, plant, and equipment, net

125,106

127,765

Operating lease assets

22,333

24,916

Intangible assets

5,627

Goodwill

6,959

6,959

Deferred tax assets

18,123

18,123

Other assets

4,715

4,850

Total assets

$

870,580

$

882,249

Liabilities and stockholders equity

Accounts payable

$

16,238

$

9,990

Accrued liabilities

93,313

99,374

Current tax liabilities

2,004

437

Other current liabilities

6,947

7,760

Total current liabilities

118,502

117,561

Long-term liabilities:

Finance lease liabilities

5,066

5,573

Operating lease liabilities

19,659

21,650

Other liabilities

10,416

11,431

Total long-term liabilities

35,141

38,654

Total liabilities

153,643

156,215

Commitments and contingencies

Stockholders’ equity:

Common stock - Ordinary shares par value £0.001; 373,709,720 shares outstanding as of June 30, 2020; 371,068,436 shares outstanding as of December 31, 2019

575

570

Additional paid-in capital

1,655,500

1,632,046

Accumulated deficit

(854,752

)

(837,959

)

Accumulated other comprehensive loss

(84,386

)

(68,623

)

Total stockholders’ equity

716,937

726,034

Total liabilities and stockholders’ equity

$

870,580

$

882,249

GW PHARMACEUTICALS PLC
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS
(in thousands, except per share amounts)
(unaudited)

Three Months Ended
June 30,

Six Months Ended
June 30,

2020

2019

2020

2019

Revenues

Product net sales

$

121,230

$

71,489

$

241,762

$

110,463

Other revenue

67

549

168

822

Total revenues

121,297

72,038

241,930

111,285

Operating expenses

Cost of product sales

8,708

6,620

19,477

11,751

Research and development

45,734

32,467

91,608

62,842

Selling, general and administrative

75,894

62,273

147,077

117,351

Total operating expenses

130,336

101,360

258,162

191,944

Loss from operations

(9,039

)

(29,322

)

(16,232

)

(80,659

)

Interest income

250

2,310

1,519

4,397

Interest expense

(297

)

(268

)

(581

)

(533

)

Other income

-

104,117

-

104,117

Foreign exchange gain

1,386

2,026

1,366

912

(Loss) income before income taxes

(7,700

)

78,863

(13,928

)

28,234

Income tax expense (benefit)

1,128

(885

)

2,865

(1,450

)

Net (loss) income

$

(8,828

)

$

79,748

$

(16,793

)

$

29,684

Net loss per share:

Basic

$

(0.02

)

$

0.21

$

(0.04

)

$

0.08

Diluted

$

(0.02

)

$

0.21

$

(0.04

)

$

0.08

Weighted average shares outstanding:

Basic

375,525

371,712

374,680

370,776

Diluted

375,525

377,435

374,680

376,674

GW PHARMACEUTICALS PLC
CONSOLIDATED STATEMENTS OF CASH FLOWS
(in thousands)
(unaudited)

Six Months Ended June 30,

2020

2019

Cash flows from operating activities

Net loss

$

(16,793

)

$

29,684

Adjustments to reconcile net loss to net cash used in operating activities:

Foreign exchange (gain) loss

(488

)

882

Share-based compensation

24,677

23,330

Depreciation and amortization

5,514

4,808

Gain from sale of priority review voucher

(104,117

)

Other

27

21

Changes in operating assets and liabilities:

Accounts receivable, net

(31,794

)

(27,924

)

Inventory

(19,669

)

(27,070

)

Prepaid expenses and other current assets

(4,312

)

(6,819

)

Other assets

1,884

1,542

Accounts payable

6,625

3,488

Current tax liabilities

2,732

619

Accrued liabilities

(599

)

13,887

Other liabilities

(2,145

)

(2,192

)

Net cash used in operating activities

(34,341

)

(89,861

)

Cash flows from investing activities

Proceeds from sale of priority review voucher

104,117

Additions to property, plant and equipment

(11,362

)

(22,515

)

Additions to capitalized software

(1,455

)

(1,017

)

Additions to intangible assets

(6,404

)

Net cash (used) provided by in investing activities

(19,221

)

80,585

Cash flows from financing activities

Proceeds from exercise of stock options

5

2,878

Payments in connection with common stock withheld for employee tax obligation

(1,223

)

Payments on finance leases

(146

)

(250

)

Payments on landlord financing obligation

(283

)

(273

)

Net cash (used in) provided by financing activities

(1,647

)

2,355

Effect of exchange rate changes on cash

(4,167

)

(893

)

Net decrease in cash and cash equivalents

(59,376

)

(7,814

)

Cash and cash equivalents at beginning of period

536,933

591,497

Cash and cash equivalents at end of period

$

477,557

$

583,683

Supplemental disclosure of cash flow information:

Income taxes paid

251

3,907

Interest paid

581

533

Supplemental disclosure of noncash information:

Property and equipment purchases in accounts payable and accrued liabilities

1,727

856

Right-of-use asset obtained in exchange for operating liabilities

275


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