Biotechnology company ImmunoGen Inc. (IMGN:NASDAQ), which concentrates its efforts on generating targeted antibody-drug conjugates (ADCs) therapies for the treatment of cancer, today provided a report detailing its recent business activities and announced financial results for the fourth quarter and year ended December 31, 2020.
The company's President and CEO Mark Enyedy commented, "Despite the challenges of the pandemic, 2020 was a transformative year for ImmunoGen...Within our portfolio, we advanced accrual in the pivotal SORAYA and confirmatory MIRASOL trials for mirvetuximab soravtansine in patients with ovarian cancer to support our projected timelines for top-line data and regulatory submissions. In addition, we established a second registration program with our CD123-targeting ADC, IMGN632, for which we received Breakthrough Therapy designation and aligned with FDA on a path to full approval in BPDCN. Furthermore, we began dosing patients in the Phase 1 study of IMGC936, our first-in-class ADAM9-targeting ADC for solid tumors, and transitioned IMGN151, our next-generation FRα-targeting ADC, into preclinical development. Finally, through a combination of business development and activity under our ATM facility, we added over $140 million to our balance sheet in the fourth quarter."
"Taken together, our pivotal programs, experienced management team, and strong balance sheet position us well to execute on our strategy and transition ImmunoGen to a fully-integrated oncology company with two products on the market in 2022," Enyedy added.
The company discussed many of the highlights and its achievements during 2020. The company noted that it had continued patient enrollment in the pivotal SORAYA and confirmatory MIRASOL trials. The firm noted also that it was successful in advancing its partnership with Huadong Medicine and had received acceptance of the investigational new drug (IND) application for mirvetuximab in China from the National Medical Products Administration (NMPA).
The company indicated that it also worked closely with the U.S. Food and Drug Administration (FDA) to formulate "a clear path to full approval for IMGN632 by amending its ongoing 801 Phase 1/2 study with a new pivotal cohort of up to 20 frontline blastic plasmacytoid dendritic cell neoplasm (BPDCN) patients."
The company stated that with enrollment complete in the SORAYA trial the first top-line pivotal data is expected to be available in Q3/21. The firm estimated that it will be a position to submit the biologics license application (BLA) before the end of December 2021 that will support potential accelerated approval in 2022. The firm further noted that the top-line data from the MIRASOL study should become available in H2/22.
The company reported that total revenues in Q4/20 increased to $85.8 million, compared to $44.9 million in Q4/19 and that for FY/20 total revenues were $132.3 million, versus $82.3 million for FY/19.
The firm stated that these revenues consisted of revenues from license and milestone fees and non-cash royalty revenue. A major component of these revenues totaling $62.4 million was recorded in Q4/20 as the company recognized $60.5 million of the upfront fee previously received under it collaboration agreement with Jazz Pharmaceuticals and $3.2 million in upfront fees received previously from other collaborative partners.
The firm indicated that in Q4/20, net income was $31.4 million, or $0.16 per diluted share, compared $4.8 million, or $0.03 per diluted share in Q4/19. The company additionally reported that for FY/20, it posted a net loss of $44.4 million, or $0.25 per diluted share, compared to a net loss of $104.1 million, or $0.70 per diluted share for FY/19.
ImmunoGen pointed out that in Q4/20, through its At-the-Market (ATM) facility, it sold approximately 20 million shares of its common stock, which generated around $100 million in gross proceeds. Similarly, the firm advised that it sold 4.5 million additional shares generating gross proceeds of around $35 million in January 2021.
ImmunoGen provided some forward guidance and stated that for FY/21 it expects total revenues in the range of $65-75 million with operating expenses in the range of $200-210 million and projects that at year-end 2021 it will have cash and cash equivalents on its balance sheet in the amount of $140-150 million.
ImmunoGen, Inc., based in Waltham, Mass., advised that it is "developing the next generation of antibody-drug conjugates (ADCs) to improve outcomes for cancer patients." The firm endeavors to generate targeted therapies with enhanced anti-tumor activity and favorable tolerability profiles in order to disrupt the progression of cancer giving patients many more good days.
ImmunoGen started the day with a market cap of around $1.6 billion with approximately 194.7 million shares outstanding and a short interest of about 14.0%. IMGN shares opened nearly 6% higher today at $8.54 (+$0.46, +32.67%) over yesterday's $8.08 closing price and reached a new 52-week high price this morning of $10.88. The stock has traded today between $8.43 and $10.88 per share and closed at $10.53 (+$2.45, +30.32%).
[NLINSERT]Disclosure:
1) Stephen Hytha compiled this article for Streetwise Reports LLC and provides services to Streetwise Reports as an independent contractor. He or members of his household own securities of the following companies mentioned in the article: None. He or members of his household are paid by the following companies mentioned in this article: None.
2) The following companies mentioned in this article are billboard sponsors of Streetwise Reports: None. Click here for important disclosures about sponsor fees.
3) Comments and opinions expressed are those of the specific experts and not of Streetwise Reports or its officers. The information provided above is for informational purposes only and is not a recommendation to buy or sell any security.
4) The article does not constitute investment advice. Each reader is encouraged to consult with his or her individual financial professional and any action a reader takes as a result of information presented here is his or her own responsibility. By opening this page, each reader accepts and agrees to Streetwise Reports' terms of use and full legal disclaimer. This article is not a solicitation for investment. Streetwise Reports does not render general or specific investment advice and the information on Streetwise Reports should not be considered a recommendation to buy or sell any security. Streetwise Reports does not endorse or recommend the business, products, services or securities of any company mentioned on Streetwise Reports.
5) From time to time, Streetwise Reports LLC and its directors, officers, employees or members of their families, as well as persons interviewed for articles and interviews on the site, may have a long or short position in securities mentioned. Directors, officers, employees or members of their immediate families are prohibited from making purchases and/or sales of those securities in the open market or otherwise from the time of the decision to publish an article until three business days after the publication of the article. The foregoing prohibition does not apply to articles that in substance only restate previously published company releases.
6) This article does not constitute medical advice. Officers, employees and contributors to Streetwise Reports are not licensed medical professionals. Readers should always contact their healthcare professionals for medical advice.