ImmunoGen (IMGN) reported earnings on Friday, but except for its cash runway, the biotech's financials aren't nearly as important as plans for its pipeline.
ImmunoGen results: The only number that really matters
Metric |
Sept. 30, 2016 |
June 30, 2016 |
QOQ Decline |
---|---|---|---|
Cash and equivalents |
$196 million |
$245 million |
(20%) |
What happened with ImmunoGen this quarter?
- At the end of September, management decided to reduce its workforce by 17%, focusing on mirvetuximab soravtansine, IMGN779, and IMGN632 while partnering its non-core B-cell lymphoma program to reduce its cash burn. Management thinks the new focus will push its cash runway through its interim peak at phase 3 data for mirvetuximab soravtansine, extending into mid-2018.
- That phase 3 trial, dubbed FORWARD I, for mirvetuximab soravtansine in platinum-resistant ovarian cancer is on track to begin before the end of the year.
- ImmunoGen expects to end the year with $165 million and $170 million in the bank, implying a cash burn rate of $26 million to $31 million, but that rate will increase in coming quarters as it ramps up its spending on clinical trials.
- Its phase 2 trial, FORWARD II, which looks at mirvetuximab soravtansine in combination with other treatments, is still enrolling patients.
What management had to say
On the potential to sell its non-core assets, ImmunoGen CEO Mark Enyedy said, "We have some preliminary conversations ongoing at this point, and there's not much else to say on that point." Clearly, generating some non-dilutive cash would be useful, but investors are just going to have to wait.
Much has been made about ImmunoGen having enough cash to get through the interim peak at the FORWARD I trial data, but Anna Berkenblit, ImmunoGen's chief medical officer, noted that "it's just a futility analysis because progression free survivals is the primary end point. We do not have an early stop for efficacy." Knowing that the trial won't end early will remove some risk from ImmunoGen, but the interim look doesn't offer a huge upside since it can't be stopped early for efficacy.
Looking forward
While investors won't get data from FORWARD I for some time, ImmunoGen expects to start reporting data from FORWARD II next year, perhaps at the American Society of Clinical Research (ASCO) meeting in June. If mirvetuximab soravtansine works well in combination with currently approved drugs, such as Roche's Avastin and Merck's Keytruda, investors should have more confidence that mirvetuximab soravtansine will work on its own in later-stage patients who have failed other treatments -- the patients in the FORWARD I trial.
Before then, at the American Society of Hematology (ASH) meeting next month, investors will get a look at preclinical data for IMGN779 and IMGN632. IMGN779 is already being tested in a phase 1 trial in patients with acute myeloid leukemia. A phase 1 trial for IMGN632 is scheduled to start in 2017.