Assembly Biosciences Reports Fourth Quarter and Year End 2018 Financial Results
“Assembly has achieved many significant milestones over the past year across both our HBV and microbiome programs,” stated
Mr. Small further commented, “In addition, we are pleased to announce the initiation of a Phase 1b study of ABI-M201, the first clinical candidate from our collaboration with
Fourth Quarter 2018 and Recent Highlights
- Assembly presented final results of the Phase 1b study of ABI-H0731 at the AASLD Annual Meeting in
San Franciscoin November 2018. Data showed that 731 was well tolerated, with substantial reductions in both HBV DNA and RNA, distinguishing it from standard of care nucleos(t)ide therapy. The presentation was designated a “Best of AASLD 2018” selection.
November 2018, Assembly initiated a Phase 1a study of ABI-H2158 and selected ABI-H3733 as its third core inhibitor candidate for development.
January 2019, Assembly completed enrollment of two 24-week Phase 2a studies evaluating ABI-H0731, the Company’s lead HBV core inhibitor. The ABI-H0731-201 “viral antigen” proof-of-concept study enrolled both HBeAg positive and negative patients whose viral load was already suppressed on active nucleos(t)ide (‘Nuc’) therapy. The ABI-H0731-202 “viral load” kinetic study enrolled treatment-naïve HBeAg positive patients and is designed to evaluate the de novo combination of ABI-H0731 and ‘Nuc’ therapy (entecavir) to ‘Nuc’ monotherapy alone. Patients from both studies have the option to roll-over into a 12-month open label extension study, ABI-H0731-211, and receive a combination of ABI-H0731 with ongoing ‘Nuc’ therapy.
February 2019, Assembly and Allerganinitiated a Phase 1b study of ABI-M201 (M201) in patients with mildly to moderately active ulcerative colitis (UC). M201 is the first oral live biotherapeutic product (LBP) to enter clinical development under the collaboration, and consists of a rationally designed consortium of gut commensal bacteria specifically selected for functional attributes relevant in the treatment of UC. M201 will be delivered orally, utilizing Assembly’s Gemicel® capsule-in-capsule delivery system designed for targeted two-stage delivery into the lower gastrointestinal tract. The Phase 1b study is a randomized, double-blind, and placebo-controlled trial to evaluate safety, efficacy and exploratory endpoints.
Anticipated Milestones and Events
- Annual Meeting of the
European Association for the Study of Liver Disease(EASL) in Vienna, Austria, April 10-14, 2019– Regular submission acceptances:
○ Oral presentation, “Preclinical profile of HBV core protein inhibitor, ABI-H3733, a potent inhibitor of cccDNA generation in HBV infected cells”.
○ Poster presentation, “Rapid turnover of HBV cccDNA in nucleoside-treated chronic hepatitis B patients during drug resistance emergence and breakthrough”.
○ Initial data from Phase 2a combination studies in HBV patients expected in Q2 2019.
○ Final six month data from Phase 2a combination studies expected in H2 2019.
○ Initiation of Phase 1b study in HBV patients expected in Q2 2019.
○ Preclinical profile to be featured in oral presentation at EASL 2019.
○ Ongoing Phase 1b study in patients with mildly to moderately active UC.
- Microbiome Platform
○ Leveraging discovery, development and manufacturing capabilities to advance new proprietary LBP candidates for other disease indications.
Fourth Quarter 2018 and Year End Financial Results
- Cash, cash equivalents and marketable securities were approximately
$218.1 millionas of December 31, 2018compared to approximately $233.9 millionas of the three months ended September 30, 2018and approximately $123.3 millionas of the year ended December 31, 2017.
- Revenues consisting of revenue from collaborative research were approximately
$3.7 millionfor the three months ended December 31, 2018compared to $3.3 millionfor the same period in 2017 and approximately $14.8 millionfor the year ended December 31, 2018compared to approximately $9.0 millionin 2017. The increase was related to an increase in Allergan-related activities and expense reimbursement.
- Research and development expenses, excluding stock-based compensation expense, were approximately
$18.1 millionfor the three months ended December 31, 2018compared to approximately $8.9 millionin 2017 and approximately $60.9 millionfor the year ended December 31, 2018compared to approximately $38.8 millionin 2017. The year end increase was primarily due to an increase of approximately $18.3 millionin research and development expenses related to the HBV program and an increase of approximately $3.9 millionin research and development expenses related to the microbiome program. Stock-based compensation expense was approximately $3.1 millionfor the three months ended December 31, 2018compared to approximately $1.7 millionfor the same period in 2017 and approximately $11.8 millionfor the year ended December 31, 2018as compared to $5.4 millionin 2017.
- General and administrative expenses, excluding stock-based compensation expense, were approximately
$6.3 millionfor the three months ended December 31, 2018compared to $3.9 millionfor the same period in 2017, and approximately $18.1 millionfor the year ended December 31, 2018as compared to approximately $13.8 millionin 2017. The increase was primarily due to increased headcount across the organization. Stock-based compensation expense was approximately $3.7 millionfor the three months ended December 31, 2018compared to approximately $1.1 millionfor the same period in 2017 and approximately $16.7 millionfor the year ended December 31, 2018as compared to approximately $3.2 millionin 2017. This increase was primarily due to expenses related to non-cash, stock-based compensation grants and employee incentive programs including the 2018 Employee Stock Purchase Plan.
- Net loss attributable to common stockholders was approximately
$26.1 million, or $1.03per basic and diluted share, for the three months ended December 31, 2018compared to approximately $3.0 million, or $0.16per basic and diluted share, for the same period in 2017. For the year ended December 31, 2018, net loss was approximately $90.8 million, or $3.98per basic and diluted share compared to approximately $42.6 million, or $2.41per basic and diluted share, for the year ended December 31, 2017. The increase was primarily due to an increase in research and development expenses related to the HBV program, expenses related to non-cash, stock-based compensation, employee incentive programs, increased headcount across the organization and a one-time income tax benefit in 2017.
About Assembly Biosciences
The information in this press release contains forward-looking statements regarding future events, including statements about the clinical and therapeutic potential of core inhibitors, including ABI-H0731, ABI-H2158 and ABI-H3733 and live biotherapeutic product candidate ABI-M201, Assembly’s development programs, the initiation, progress and results of Assembly’s ongoing and planned clinical studies and the timing of these events. Certain forward-looking statements may be identified by reference to a future period or by use of forward-looking terminology such as “plan,” “upcoming,” “anticipated,” “will,” “expected,” and “potential.” Assembly intends such forward-looking statements to be covered by the safe harbor provisions contained in Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. Actual results or developments may differ materially from those projected or implied in these forward-looking statements. More information about the risks and uncertainties faced by Assembly are more fully detailed under the heading “Risk Factors” in Assembly's Annual Report on Form 10-K for the year ended December 31, 2018 filed with the Securities and Exchange Commission. Except as required by law, Assembly assumes no obligation to update publicly any forward-looking statements, whether as a result of new information, future events or otherwise.
|Assembly Biosciences, Inc.|
|Condensed Consolidated Balance Sheets|
|As of December 31,|
|Cash and cash equivalents||$||41,471||$||82,033|
|Marketable securities, at fair value||176,609||37,914|
|Accounts receivable from collaboration||2,430||2,274|
|Prepaid expenses and other current assets||1,992||898|
|Total current assets||222,502||123,119|
|Marketable securities, at fair value||-||3,347|
|Property, plant and equipment, net||557||860|
|Indefinite-lived intangible asset||29,000||29,000|
|Total long-term assets||45,543||46,185|
|LIABILITIES AND STOCKHOLDERS' EQUITY|
|Deferred revenue - short-term||5,100||5,229|
|Total current liabilities||18,472||13,492|
|Deferred tax liabilities||3,252||2,136|
|Deferred revenue - long-term||35,560||40,556|
|Total long-term liabilities||38,920||42,692|
|Commitments and contingencies|
|Preferred stock, $0.001 par value; 5,000,000 shares authorized; 0 shares issued and outstanding||-||-|
|Common stock, $0.001 par value; 100,000,000 and 50,000,000 shares authorized as of December 31, 2018 and December 31, 2017; 25,495,425 and 20,137,974 shares issued and outstanding as of December 31, 2018 and December 31, 2017, respectively||25||20|
|Additional paid-in capital||552,762||364,528|
|Accumulated other comprehensive loss||(347||)||(392||)|
|Total stockholders' equity||210,653||113,120|
|Total liabilities and stockholders' equity||$||268,045||$||169,304|
|Assembly Biosciences, Inc.|
|Condensed Consolidated Statements of Operations and Comprehensive Loss|
|Year Ended December 31,|
|Research and development||72,741||44,225||33,093|
|General and administrative||34,798||17,021||12,185|
|Total operating expenses||107,539||61,246||45,278|
|Loss from operations||(92,735||)||(52,227||)||(45,278||)|
|Other income (expenses)|
|Interest and other income||3,083||983||1,539|
|Realized loss from marketable securities||-||(615||)||(1,140||)|
|Total other income||3,083||368||399|
|Loss before income taxes||(89,652||)||(51,859||)||(44,879||)|
|Income tax (expenses) benefit||(1,099||)||9,050||618|
|Other comprehensive (loss) income|
|Unrealized gain (loss) on marketable securities, net of tax||45||209||221|
|Net loss per share, basic and diluted||$||(3.98||)||$||(2.41||)||$||(2.57||)|
|Weighted average common shares outstanding, basic and diluted||22,801,644||17,750,380||17,226,245|
Source: Assembly Biosciences, Inc.