-
Rani Therapeutics Reports Fourth Quarter and Full Year 2021 Financial Results; Provides Corporate Update
来源: Nasdaq GlobeNewswire / 29 3月 2022 15:05:00 America/Chicago
- Initiated a Phase 1 clinical trial of RT-102 for the potential treatment of osteoporosis -
- Unveiled the high-capacity RaniPill™ HC, capable of delivering payloads of up to 20 mg -
- Strengthened Board with the appointments of Lyn Baranowski and Lisa Rometty –
- Conference call and webcast today at 4:30 p.m. ET -
SAN JOSE, Calif., March 29, 2022 (GLOBE NEWSWIRE) -- Rani Therapeutics Holdings, Inc. (“Rani Therapeutics” or “Rani”) (Nasdaq: RANI), a clinical stage biotherapeutics company focused on the oral delivery of biologics, today reported financial results for the fourth quarter and full year ended December 31, 2021 and provided a corporate update.
“The year 2021 and the subsequent months that have passed have been a productive period for Rani. We refined and progressed our development pipeline; made strides on RaniPill HC, the high capacity version of our RaniPill platform; bolstered our balance sheet through a successful IPO; and strengthened our board and management with the addition of key personnel,” said Talat Imran, Chief Executive Officer of Rani Therapeutics. “Looking ahead to the rest of 2022, we expect to announce topline results from our Phase 1 trial of RT-102 and initiate an additional Phase 1 trial – the company’s third – in the second half of the year. We also expect to make progress with the RaniPill HC, which adds over 50 potential biologic drug candidates as opportunities for internal development or partnership.”
Fourth Quarter and Subsequent Highlights
- Initiated a Phase 1 Clinical Study of RT-102. In March 2022, Rani announced the initiation of a Phase 1 clinical study of RT-102, a RaniPill capsule containing parathyroid hormone for the treatment of osteoporosis, in Australia. The single-center, open label, Phase 1 study is evaluating the pharmacokinetics, safety and tolerability of RT-102 administered in healthy adult women volunteers. Preclinical data of RT-102 demonstrated a pharmacokinetic profile comparable to published data for once-daily PTH injections for the treatment of osteoporosis.
- Unveiled the RaniPill High Capacity (HC). In February 2022, Rani announced the development of the RaniPill HC, an oral device capable of delivering therapeutic payloads of up to 500%-plus more than the original RaniPill capsule. In preclinical testing in a canine model using an adalimumab payload, the RaniPill HC deployed successfully and yielded a PK profile proportional to historical data obtained with adalimumab delivered via the original RaniPill capsule.
- Completed Preclinical GLP 7-Day Repeat Oral Administration Study. In November 2021, Rani completed a GLP 7-day repeat oral administration study evaluating the safety and tolerability of RT-102 in canines. In the study, no safety events were observed.
- Additions to the Board of Directors. In January 2022 and November 2021, Rani strengthened its Board of Directors with the appointments of Lisa Rometty and Lyn Baranowski, respectively. Ms. Rometty has more than two decades of global commercialization and product development experience in the biotechnology and healthcare space. Ms. Baranowski is a seasoned biotechnology executive with a diverse set of knowledge around product portfolios and therapeutic areas.
Expected Near-Term Milestones
- Topline Phase 1 RT-102 data readout expected in 2H 2022
- Initiation of an additional Phase 1 clinical study expected in 2H 2022
Full Year 2021 Financial Results
- Cash and cash equivalents as of December 31, 2021 were $117.5 million, compared to $73.1 million as of December 31, 2020. Rani expects its cash and cash equivalents balance to be sufficient to fund its operating expenses and capital expenditure requirements at least until the end of 2023.
- Research and development (R&D) expenses for the three and twelve months ended December 31, 2021 were $7.4 million and $26.5 million, respectively, compared to $3.3 million and $12.0 million for the same periods in 2020, respectively. The increases were primarily attributed to higher compensation and benefits due to the increase in headcount, including $8.2 million for the full-year of non-cash equity-based compensation expense; of which $6.2 million was recognized in connection with the company’s IPO and related corporate reorganization in the third quarter of 2021.
- General and administrative expenses for the three and twelve months ended December 31, 2021 were $5.9 million and $27.8 million, respectively, compared to $1.8 million and $5.0 million for the same periods in 2020, respectively. The increases were primarily attributed to the public company related costs and higher compensation and benefits due to the increase in headcount, including $14.4 million for the full-year of non-cash equity-based compensation expense; of which $10.7 million was recognized in connection with the company’s IPO and related corporate reorganization in the third quarter of 2021.
- Net loss for the three and twelve months ended December 31, 2021 was $13.3 million and $53.1 million, respectively, compared to $5.8 million and $16.7 million for the same periods in 2020, respectively.
Conference Call
Rani will host a corresponding conference call and live webcast at 1:30 p.m. PT / 4:30 p.m. ET on March 29, 2022 to discuss the results and provide a business update. Individuals interested in listening to the live conference call may do so by dialing (844) 605-7369 for domestic callers, or (929) 517-0917 for international callers and reference conference ID: 7192045; or from the webcast link in the investor relations section of the company's website at: www.ranitherapeutics.com.
A webcast replay will be available in the investor relations section on the company's website for 90 days following the completion of the call.
Rani Therapeutics
Rani Therapeutics is a clinical stage biotherapeutics company focused on advancing technologies to enable the development of orally administered biologics. Rani has developed the RaniPill™ capsule, which is a novel, proprietary and patented platform technology, intended to replace subcutaneous injection of biologics with oral dosing. Rani has successfully conducted several preclinical and clinical studies to evaluate safety, tolerability and bioavailability using the RaniPill™ capsule. For more information, visit www.ranitherapeutics.com.
Forward-Looking Statements
Statements contained in this press release regarding matters that are not historical facts are “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995. Such forward-looking statements include statements regarding, among other things, the timing of topline results from Rani’s Phase 1 trial of RT-102, the expected initiation of an additional Phase 1 trial of another product candidate in the second half of 2022, expected progress with the RaniPill HC platform, and potential expansion of Rani’s prospective opportunity, alone or in partnership, to an additional 50 biologics across multiple new indications, Rani’s development and advancement of its RaniPill capsule technology, the impact of its technology on medical treatment, Rani’s advancement of its preclinical and clinical programs and timing of results, customer acceptance of the RaniPill capsule technology, the potential benefits of the RaniPill capsule technology, Rani’s ability to attract and retain talent, Rani’s prospects for entering into strategic partnerships or transactions, and Rani’s growth as a company. Because such statements are subject to risks and uncertainties, actual results may differ materially from those expressed or implied by such forward-looking statements. Words such as “may,” “could,” “prospective,” “look forward,” “progress,” “advance” and similar expressions are intended to identify forward-looking statements. These forward-looking statements are based upon Rani’s current expectations and involve assumptions that may never materialize or may prove to be incorrect. Actual results could differ materially from those anticipated in such forward-looking statements as a result of various risks and uncertainties, which include, without limitation, risks and uncertainties associated with Rani’s business in general, the impact of the COVID-19 pandemic, and the other risks described in Rani’s filings with the Securities and Exchange Commission. All forward-looking statements contained in this press release speak only as of the date on which they were made and are based on management’s assumptions and estimates as of such date. Rani undertakes no obligation to update such statements to reflect events that occur or circumstances that exist after the date on which they were made, except as required by law.
Investor Contact:
investors@ranitherapeutics.com
Media Contact:
Source: Rani Therapeutics
Rani Therapeutics Holdings, Inc.
Consolidated Balance Sheets
(In Thousands, Except Par Value)Year End December 31, 2021 2020 Assets Current assets: Cash and cash equivalents $ 117,453 $ 73,058 Related party note receivable — 1,720 Prepaid expenses 2,142 167 Total current assets 119,595 74,945 Property and equipment, net 4,612 4,470 Total assets $ 124,207 $ 79,415 Liabilities, Convertible Preferred Units and Stockholders' Equity / Members’ Deficit Current liabilities: Accounts payable $ 1,080 $ 537 Related party payable 126 145 Accrued expenses 1,434 550 Deferred revenue — 2,717 Current portion of long-term debt — 1,359 Total current liabilities 2,640 5,308 Preferred unit warrant liability — 320 Long-term debt, less current portion — 2,412 Total liabilities 2,640 8,040 Commitments and contingencies Convertible preferred units — 184,714 Stockholders' equity / (members’ deficit): Common units — 664 Preferred stock, $0.0001 par value - 20,000 shares authorized; none issued and outstanding as of December 31, 2021 — — Class A common stock, $0.0001 par value - 800,000 shares authorized; 19,712 issued and outstanding as of December 31, 2021 2 — Class B common stock, $0.0001 par value - 40,000 shares authorized; 29,290 issued and outstanding as of December 31, 2021 3 — Class C common stock, $0.0001 par value - 20,000 shares authorized; none issued and outstanding as of December 31, 2021 — — Additional paid-in capital 55,737 — Accumulated deficit (8,331 ) (114,003 ) Total stockholders' equity attributable to Rani Therapeutics Holdings, Inc. / (members' deficit) 47,411 (113,339 ) Non-controlling interest 74,156 — Total stockholders' equity / (members' deficit) 121,567 (113,339 ) Total liabilities, convertible preferred units and stockholders' equity / (members' deficit) $ 124,207 $ 79,415 Rani Therapeutics Holdings, Inc.
Consolidated Statements of Operations and Comprehensive Loss
(In Thousands, Except Per Share Amounts)Three Months Ended December 31, Year Ended December 31, 2021 2020 2021 2020 Contract revenue $ — $ 210 $ 2,717 $ 462 Operating expenses Research and development 7,417 3,336 26,482 12,044 General and administrative 5,945 1,818 27,834 4,962 Total operating expenses $ 13,362 $ 5,154 $ 54,316 $ 17,006 Loss from operations (13,362 ) (4,944 ) (51,599 ) (16,544 ) Other income (expense), net Interest income 16 (24 ) 89 63 Loss on extinguishment of debt — — (700 ) — Interest expense and other, net 1 (58 ) (466 ) (124 ) Change in estimated fair value of preferred unit warrant — (718 ) (371 ) (63 ) Loss before income taxes (13,345 ) (5,744 ) (53,047 ) (16,668 ) Income tax expense 40 (12 ) (41 ) (35 ) Net loss and comprehensive loss $ (13,305 ) $ (5,756 ) $ (53,088 ) $ (16,703 ) Net loss attributable to non-controlling interest (8,116 ) (5,756 ) (44,757 ) (16,703 ) Net loss attributable to Rani Therapeutics Holdings, Inc. $ (5,189 ) $ — $ (8,331 ) $ — Net loss per Class A common share attributable to Rani Therapeutics Holdings, Inc., basic and diluted $ (0.27 ) $ (0.43 ) Weighted-average Class A common shares outstanding—basic and diluted 19,439 19,534
- Initiated a Phase 1 Clinical Study of RT-102. In March 2022, Rani announced the initiation of a Phase 1 clinical study of RT-102, a RaniPill capsule containing parathyroid hormone for the treatment of osteoporosis, in Australia. The single-center, open label, Phase 1 study is evaluating the pharmacokinetics, safety and tolerability of RT-102 administered in healthy adult women volunteers. Preclinical data of RT-102 demonstrated a pharmacokinetic profile comparable to published data for once-daily PTH injections for the treatment of osteoporosis.