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Passage Bio Reports Third Quarter 2021 Financial Results and Provides Recent Business Highlights - On track to report initial safety and 30-day biomarker data for cohort 1 from Imagine-1 global Phase 1/2 trial for PBGM01

Key Takeaway: Passage Bio Reports Third Quarter 2021 Financial Results and Provides Recent Business Highlights Philadelphia, PA - November 4, 2021 - Passage Bio, Inc. (Nasdaq: PASG), a clinical-stage genetic medicines company focused on developing transformative therapies for central nervous

Full Press Release Details

Passage Bio Reports Third Quarter 2021 Financial Results and Provides Recent Business Highlights
Philadelphia, PA - November 4, 2021 - Passage Bio, Inc. (Nasdaq: PASG), a clinical-stage genetic medicines company focused on developing transformative therapies for central nervous system disorders, today reported financial results for the third quarter ended September 30, 2021 and provided recent business highlights.
"We ended the quarter well-positioned to deliver on multiple upcoming catalysts, including reporting first-in-human data from our Imagine-1 global Phase 1/2 trial for PBGM01 for the treatment of infantile GM1 gangliosidosis before the end of year," said Bruce Goldsmith, Ph.D., president and chief executive officer of Passage Bio. "We also have successfully activated multiple clinical sites and are continuously expanding our patient identification initiatives across each of our global clinical programs. This paves the way for us to continue to advance Imagine-1 and dose the first participants before year-end in our programs for Krabbe disease and frontotemporal dementia with granulin mutations.
"As we close this year, we remain steadfastly focused on strong execution of our three clinical programs, while continuing to progress our robust genetic medicines pipeline targeting CNS disorders affecting both rare and large patient populations."
Anticipated Upcoming Milestones
Third Quarter 2021 Financial Results
Conference Call Details
Passage Bio will host a conference call and webcast today at 8:30 a.m. ET. To access the live conference call, please dial 833-528-0605 (domestic) or 830-221-9711 (international) and reference conference ID number 2985094. A live audio webcast of the event will be available on the Investors & News section of Passage Bio's website at investors.passagebio.com. The archived webcast will be available on Passage Bio's website approximately two hours after the completion of the event and for 30 days following the call.
At Passage Bio (Nasdaq: PASG), we are on a mission to provide life-transforming genetic medicines for patients with CNS diseases that replace their suffering with boundless possibility, all while building lasting relationships with the communities we serve. Based in Philadelphia, PA, our company has established a strategic collaboration and licensing agreement with the renowned University of Pennsylvania's Gene Therapy Program to conduct our discovery and IND-enabling preclinical work. This provides our team with enhanced access to a broad portfolio of gene therapy candidates and future gene therapy innovations that we then pair with our deep clinical, regulatory, manufacturing and
commercial expertise to rapidly advance our robust pipeline of optimized gene therapies into clinical testing. As we work with speed and tenacity, we are always mindful of patients who may be able to benefit from our therapies. More information is available at www.passagebio.com.
Forward-Looking Statements
This press release contains "forward-looking statements" within the meaning of, and made pursuant to the safe harbor provisions of, the Private Securities Litigation Reform Act of 1995, including, but not limited to: our expectations about timing and execution of anticipated milestones, including initiation of clinical trials and the availability of clinical data from such trials; our expectations about our collaborators' and partners' ability to execute key initiatives; our expectations about manufacturing plans and strategies; our expectations about cash runway; and the ability of our lead product candidates to treat their respective target monogenic CNS disorders. These forward-looking statements may be accompanied by such words as "aim," "anticipate," "believe," "could," "estimate," "expect," "forecast," "goal," "intend," "may," "might," "plan," "potential," "possible," "will," "would," and other words and terms of similar meaning. These statements involve risks and uncertainties that could cause actual results to differ materially from those reflected in such statements, including: our ability to develop and obtain regulatory approval for our product candidates; the timing and results of preclinical studies and clinical trials; risks associated with clinical trials, including our ability to adequately manage clinical activities, unexpected concerns that may arise from additional data or analysis obtained during clinical trials, regulatory authorities may require additional information or further studies, or may fail to approve or may delay approval of our drug candidates; the occurrence of adverse safety events; the risk that positive results in a preclinical study or clinical trial may not be replicated in subsequent trials or success in early stage clinical trials may not be predictive of results in later stage clinical trials; failure to protect and enforce our intellectual property, and other proprietary rights; our dependence on collaborators and other third parties for the development and manufacture of product candidates and other aspects of our business, which are outside of our full control; risks associated with current and potential delays, work stoppages, or supply chain disruptions caused by the coronavirus pandemic; and the other risks and uncertainties that are described in the Risk Factors section in documents the company files from time to time with the Securities and Exchange Commission (SEC), and other reports as filed with the SEC. Passage Bio undertakes no obligation to publicly update any forward-looking statement, whether written or oral, that may be made from time to time, whether as a result of new information, future developments or otherwise.
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(in thousands, except share data) September 30, 2021 December 31, 2020
Assets
Current assets:
Cash and cash equivalents $ 162,890 $ 135,002
Marketable securities 191,511 169,815
Prepaid expenses and other current assets 3,132 1,405
Prepaid research and development 8,935 10,961
Total current assets 366,468 317,183
Property and equipment, net 17,767 2,795
Other assets 6,706 8,029
Total assets $ 390,941 $ 328,007
Liabilities and stockholders' equity
Current liabilities:
Accounts payable $ 8,978 $ 5,265
Accrued expenses and other current liabilities 13,272 15,910
Total current liabilities 22,250 21,175
Deferred rent 6,464 2,077
Other liabilities - 41
Total liabilities 28,714 23,293
Commitments and Contingencies
Stockholders' equity:
Common stock, $0.0001 par value: 300,000,000 shares authorized; 54,106,911 shares issued and 54,016,499 shares outstanding at September 30, 2021 and 45,917,084 shares issued and 45,614,807 shares outstanding at December 31, 2020 5 4
Additional paid in capital 667,316 475,617
Accumulated other comprehensive income (loss) 33 (12)
Accumulated deficit (305,127) (170,895)
Total stockholders' equity 362,227 304,714
Total liabilities and stockholders' equity $ 390,941 $ 328,007
Statements of Operations and Comprehensive Loss
Three Months Ended September 30, Nine Months Ended September 30,
(in thousands, except share and per share data) 2021 2020 2021 2020
Operating expenses:
Research and development $ 26,623 $ 20,837 $ 84,705 $ 53,856
Acquired in process research and development 5,500 - 7,000 -
General and administrative 14,978 7,793 42,864 19,990
Loss from operations (47,101) (28,630) (134,569) (73,846)
Interest income, net 186 99 337 558
Net loss $ (46,915) $ (28,531) $ (134,232) $ (73,288)
Per share information:
Net loss per share of common stock, basic and diluted $ (0.87) $ (0.63) $ (2.53) $ (2.02)
Weighted average common shares outstanding, basic and diluted 53,995,560 45,503,794 53,080,645 36,273,495
Comprehensive loss:
Net loss $ (46,915) $ (28,531) $ (134,232) $ (73,288)
Unrealized gain (loss) on marketable securities 14 (40) 45 (40)
Comprehensive loss $ (46,901) $ (28,571) $ (134,187) $ (73,328)
Last updated: Nov 4, 2021