Geron's (GERN) Q4 Earnings And Revenues Surpass Estimates
Zacks Investment Research | Mar 12, 2020 09:33PM ET
Geron Corporation (NASDAQ:GERN) incurred a loss of 15 cents per share in fourth-quarter 2019, narrower than the Zacks Consensus Estimate of a loss of 20 cents. In the year-ago quarter, the company had incurred a loss of 4 cents per share.
Quarterly revenues came in at $0.17 million, slightly beating the Zacks Consensus Estimate of $0.14 million. Notably, the top line comprised royalty and license fee revenues received under various non-imetelstat license agreements. In the year-ago quarter, revenues had totaled $0.38 million. Revenues declined as the number of active license agreements fell due to expiry of patents of Geron’s underlying technology.
Despite the better-than-expected results, shares of Geron were down almost 6.1% in after-hours trading on Mar 12 amid bloodbath in broader markets related to the coronavirus outbreak. In the past year, the stock has declined 39.6% compared with the industry ’s 16% decrease.
R&D expenses were $24.9 million compared with $5.1 million in the year-ago quarter as well as $11.1 million in the previous quarter. The significant year over year increase in R&D expenses was due to transition costs and higher clinical activity related to its lead pipeline candidate, imetelstat.
General and administrative expenses rose 8.2% to $5.3 million, reflecting legal costs related to patent litigations and recruitment expenses for additional headcounts.
Geron ended the fourth quarter with $159.2 million in cash and investments compared with $159.3 million at the end of the third quarter 2019.
Full Year Results
Geron incurred a loss of 36 cents in 2019 compared with loss of 15 cents in 2018. Revenues for the full year were $0.46 million, down from $1.1 million in the year-ago period.
2020 Guidance
Geron provided its guidance for 2020. The company expects full-year operating expenses to be in the range of $70-$75 million. The company expects its cash resources to be sufficient to continue with the phase III IMerge study on imetelstat in 2020 and initiate a proof-of-concept study in the year.
However, the company expects that the coronavirus pandemic may impact its enrollment timeline as well as hamper drug supply related to its clinical studies.
Pipeline Update
Following the termination of the agreement with Janssen, a subsidiary of J&J (NYSE:JNJ) , in September 2018, Geron regained global development rights to imetelstat and decided to continue developing imetelstat independently. The transition activities, including ex-U.S. clinical and regulatory responsibilities, were completed in the third quarter of 2019.
In October 2019, the company initiated dosing in the phase III study, IMerge, in patients with lower risk myelodysplastic syndromes (“MDS”). The company expects to complete enrollment by the end of 2020 and anticipates top-line data from the study in mid-2022.
Geron completed an end of phase II meeting with the FDA in the fourth quarter of 2019 related to development of imetelstat as a treatment of myelofibrosis (“MF”). Based on the FDA’s feedback, the company plans to submit a phase III study design to evaluate imetelstat in MF patients in the second quarter of 2020. Any decision related to late-stage development plans for MF will be announced by mid-2020.
The company is also planning to develop imetelstat in additional hematologic myeloid malignancies. It is planning to initiate a proof-of-concept studyby the end of the fourth quarter 2020 to evaluate imetelstat in intermediate-2 or high-risk, or higher risk, MDS and acute myeloid leukemia.
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