For investors who are already planning their investment plans for 2017, Motley Fool analysts believe that there are three biotech small-cap stocks that should not be missed and worthy of shot.
Although biotech and pharmaceutical stocks were bleak in 2016, Motley Fool's Sean Williams said that if investors are wise, they should hurry to snap up GERN, Portola Pharmaceuticals (PTLAN) and CoLucid (CLCD) because these three The stock has the potential to double next year.
1. Jielong Biomedical Company
The shares of American Jaylong Biomedical Company were sold at $2.02 this morning. According to Williams, the key drivers of Jerón's growth are top-line data from IMbark and IMerge, which are expected to be released in the second quarter of 2017. In September of this year, Jielong provided the latest research data of imetelstat, which is a special effect drug jointly developed by Yangsen Pharmaceutical for the treatment of rare blood cancer myelofibrosis. After Jansson’s additional request for internal data review of the IMbark trial, Jerón’s stock was hit hard. Yang Sen and Jie Long also said that they will stop the trial of the smaller dose, but will continue the trial of the higher dose. Such a message is enough to scare off some investors. However, Williams believes that the prospect of imetelstat is very optimistic and can compete with Incyte (INCY)'s JAK kinase inhibitor Jakafi. If it turns out that the efficacy of imetelstat is really good, it may make the stock go straight up. However, Williams pointed out that if the imetelstat test fails, it will push Jielong into the abyss.
2. Portola Pharmaceuticals
Williams said buying Portola is a gamble, but it is also worth a visit. Portola shares rose this morning at a price of $17.94. Earlier this year, Portola suffered from an unsatisfactory test result for the factor Xa anticoagulant betrixaban. At the time, clinical trials compared betrixaban and Sanofi (SNY)'s Lovenox, and the results were mixed, resulting in a fall in Portola's share price. Although betrixaban's Phase III trial data did not meet the test objectives, Portola still plans to submit a new drug application. But Williams believes that the problem is how far the test results are from important data targets. If the gap is small, will the US Food and Drug Administration (FDA) approve it without additional testing? This issue investors need to seriously consider. In August of this year, the FDA refused to issue a pass for the treatment of fatal/uncontrollable bleeding for AndexXa, so Portola suffered another setback. The FDA sent a full response letter to Portola asking for more detailed pharmaceutical information.
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