- Two New Drug Applications (NDAs) for vonoprazan-based treatment regimens for H. pylori infection were accepted for filing by FDA with six-month Priority Review granted; PDUFA target action date of
May 3, 2022 U.S. launch for both vonoprazan-based treatment regimens for H. pylori anticipated in the second half of 2022, if approved- Positive Phase 3 trial results for vonoprazan in erosive esophagitis (EE) reported in
October 2021 ; NDA submission targeted for the first quarter of 2022
“Phathom continued its strong execution through the third quarter of 2021, delivering impressive topline results from our pivotal Phase 3 PHALCON-EE study. The PHALCON-EE data adds to our excitement about vonoprazan’s potential to satisfy large unmet patient needs in the
Clinical and Regulatory Updates:
- The
U.S. Food and Drug Administration (FDA) accepted NDAs for two convenience packs containing vonoprazan-based treatment regimens for adults with H. pylori infection: vonoprazan in combination with amoxicillin and clarithromycin (“vonoprazan triple therapy”) and vonoprazan in combination with amoxicillin (“vonoprazan dual therapy”). The NDAs were granted Priority Review designation with a Prescription Drug User Fee Act (PDUFA) target action date ofMay 3, 2022 . Phathom submitted the NDAs to the FDA onSeptember 3, 2021 . The FDA previously designated vonoprazan dual and triple therapy as qualified infectious disease products (QIDPs) which, if approved, will provide vonoprazan five additional years of regulatory exclusivity. - If approved, the
U.S. commercial launch for vonoprazan dual and triple therapy is anticipated in the second half of 2022. - Vonoprazan successfully met its primary endpoints and key secondary superiority endpoints in PHALCON-EE, a pivotal Phase 3 trial evaluating vonoprazan for the healing and maintenance of healing of erosive esophagitis. Based on these results, Phathom expects to submit an NDA in the first quarter of 2022 seeking the following indications for vonoprazan: healing of all grades of EE and relief of heartburn, and maintenance of healing of all grades of EE and relief of heartburn.
- Topline results from the Phase 2 PHALCON-NERD on-demand trial evaluating various doses of vonoprazan as an on-demand therapy for patients with non-erosive reflux disease are expected in the first quarter of 2022.
Recent Business and Financial Updates:
- On
September 17, 2021 , Phathom secured an up to$200 million term loan facility from Hercules Capital (Loan Agreement). One-hundred million dollars were drawn at closing and an additional$50 million became available upon the receipt of positive topline results in PHALCON-EE. The final$50 million tranche will become available upon the occurrence of both FDA approval of a vonoprazan-based regimen for the treatment of H. pylori, and FDA acceptance of filing of an NDA for vonoprazan for the treatment of erosive esophagitis.
Third Quarter 2021 Financial Results:
- Third quarter 2021 net loss was
$36.7 million compared to$34.1 million for the third quarter of 2020. - Third quarter 2021 net loss included a non-cash charge related to stock-based compensation of
$4.4 million compared to the third quarter of 2020 non-cash charge related to stock-based compensation of$2.1 million . - Third quarter 2021 research and development expenses decreased to
$16.6 million compared to$25.8 million for the third quarter 2020 due to lower clinical trial costs, partially offset by higher regulatory and personnel-related expenses. - Third quarter 2021 general and administrative expenses increased to
$16.5 million compared to$7.1 million for the third quarter of 2020 due to the ongoing buildout of administrative and commercial functions. - Third quarter 2021 other expenses increased by
$2.3 million compared to the third quarter of 2020 due to a$2.0 million charge related to the early extinguishment of Phathom’s previous debt facility replaced by the Loan Agreement. - As of
September 30, 2021 , cash and cash equivalents were$224.6 million . Cash and cash equivalents combined with the future drawdown of the remaining$100 million under the Loan Agreement are expected to be sufficient to meet anticipated cash requirements into mid-2023 based on current operating plans.
About Vonoprazan
Vonoprazan is an investigational, oral small molecule potassium-competitive acid blocker (P-CAB). P-CABs are a novel class of medicines that block acid secretion in the stomach. Vonoprazan has shown the potential to have rapid, potent, and durable anti-secretory effects as a single agent in the treatment of gastroesophageal reflux disease (GERD) and in combination with antibiotics for the treatment of Helicobacter pylori (H. pylori) infection. The
About
Forward Looking Statements
The Company cautions you that statements contained in this press release regarding matters that are not historical facts are forward-looking statements. These statements are based on the Company’s current beliefs and expectations. Such forward-looking statements include, but are not limited to, statements regarding the expected availability of topline results from the PHALCON-NERD on demand clinical trial, the expected submission of an NDA for the healing of all grades of EE and relief of heartburn, and maintenance of healing of all grades of EE and relief of heartburn, the expected approval of NDAs for vonoprazan-based treatments for the treatment of H. pylori infection, and the Company’s ability to access additional capital under the Loan Agreement. The inclusion of forward-looking statements should not be regarded as a representation by the Company that any of its plans will be achieved. Actual results may differ from those set forth in this press release due to the risks and uncertainties inherent in the Company’s business, including, without limitation: reported top-line data is based on preliminary analysis of key efficacy and safety data is subject to more audit and verification procedures that could result in material changes in the final data; the Company may experience delays submitting an NDA including in the event that the FDA does not agree with the Company’s interpretation of the data or feedback from the FDA that may be inconsistent with feedback received at prior meetings with the FDA; Phathom’s ability to access additional capital under the Loan Agreement is subject to certain conditions including verification by the lender that the clinical milestone has been met; the Company’s dependence on third parties in connection with product manufacturing, research and preclinical and clinical testing; regulatory developments in
CONTACTS
Media Contact:
1-877-742-8466
media@phathompharma.com
Investor Contact:
1-877-742-8466
ir@phathompharma.com
Balance Sheets
(Unaudited)
(in thousands, except share and par value amounts)
2021 | 2020 | |||||||
Assets | ||||||||
Current assets: | ||||||||
Cash and cash equivalents | $ | 224,618 | $ | 287,496 | ||||
Prepaid expenses and other current assets (including related party amounts of | 695 | 3,872 | ||||||
Total current assets | 225,313 | 291,368 | ||||||
Property, plant and equipment, net | 692 | 986 | ||||||
Operating lease right-of-use assets | 2,031 | 2,373 | ||||||
Other long-term assets | 341 | 384 | ||||||
Total assets | $ | 228,377 | $ | 295,111 | ||||
Liabilities and Stockholders’ Equity | ||||||||
Current liabilities: | ||||||||
Accounts payable (including related party amounts of | $ | 5,582 | $ | 16,782 | ||||
Accrued clinical trial expenses | 10,491 | 19,997 | ||||||
Accrued expenses (including related party amounts of | 11,040 | 10,606 | ||||||
Accrued interest | 214 | 312 | ||||||
Current portion of long-term debt | — | 7,353 | ||||||
Operating lease liabilities, current | 484 | 474 | ||||||
Total current liabilities | 27,811 | 55,524 | ||||||
Long-term debt, net of discount | 88,305 | 39,634 | ||||||
Operating lease liabilities | 1,280 | 1,557 | ||||||
Other long-term liabilities | 7,500 | 4,125 | ||||||
Total liabilities | 124,896 | 100,840 | ||||||
Stockholders’ equity: | ||||||||
Preferred stock, outstanding at | - | - | ||||||
Common stock, | 3 | 3 | ||||||
Additional paid-in capital | 597,022 | 579,755 | ||||||
Accumulated deficit | (493,544 | ) | (385,487 | ) | ||||
Total stockholders’ equity | 103,481 | 194,271 | ||||||
Total liabilities and stockholders’ equity | $ | 228,377 | $ | 295,111 |
Statements of Operations and Comprehensive Loss
(Unaudited)
(in thousands, except share and per share amounts)
Three Months Ended | Nine Months Ended | |||||||||||||||
2021 | 2020 | 2021 | 2020 | |||||||||||||
Operating expenses: | ||||||||||||||||
Research and development (includes related party amounts of | $ | 16,608 | $ | 25,770 | $ | 58,786 | $ | 56,494 | ||||||||
General and administrative (includes related party amounts of | 16,529 | 7,060 | 43,254 | 16,732 | ||||||||||||
Total operating expenses | 33,137 | 32,830 | 102,040 | 73,226 | ||||||||||||
Loss from operations | (33,137 | ) | (32,830 | ) | (102,040 | ) | (73,226 | ) | ||||||||
Other income (expense): | ||||||||||||||||
Interest income | 8 | 15 | 35 | 1,075 | ||||||||||||
Interest expense | (1,485 | ) | (1,286 | ) | (4,013 | ) | (3,286 | ) | ||||||||
Change in fair value of warrant liabilities | — | — | — | 95 | ||||||||||||
Other income (expense) | (2,048 | ) | (4 | ) | (2,039 | ) | (5 | ) | ||||||||
Total other income (expense) | (3,525 | ) | (1,275 | ) | (6,017 | ) | (2,121 | ) | ||||||||
Net loss and comprehensive loss | $ | (36,662 | ) | $ | (34,105 | ) | $ | (108,057 | ) | $ | (75,347 | ) | ||||
Net loss per share, basic and diluted | $ | (0.98 | ) | $ | (1.02 | ) | $ | (2.94 | ) | $ | (2.29 | ) | ||||
Weighted-average shares of common stock outstanding, basic and diluted | 37,299,351 | 33,366,237 | 36,748,492 | 32,946,128 |
Source:
2021 GlobeNewswire, Inc., source