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Pfizer's Arthritis Drug Gets FDA Nod for Ulcerative Colitis
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Pfizer Inc. (PFE - Free Report) announced that the FDA has approved the label expansion of its JAK inhibitor, Xeljanz (tofacitinib), to include a new indication – moderately to severely active ulcerative colitis (“UC”). The drug is approved for the treatment of adult patients with recommended a dose of 10 mg twice-daily for at least eight weeks.
The approval was expected as the FDA Gastrointestinal Drugs Advisory Committee had adopted a positive vote in a meeting in March recommending the approval of the supplemental new drug application (sNDA) filed in July last year seeking label expansion of Xeljanz in UC.
Xeljanz is already marketed for the treatment of rheumatoid arthritis and active psoriatic arthritis. In the first quarter of 2018, Xeljanz sales were $326 million, up 30.4% from the year-ago period. The label expansion in the UC indication is likely to boost its sales further.
Shares of Pfizer have lost 0.5% so far this year, compared with a 6% decrease for the industry it belongs to.
The approval was based on data from three pivotal studies – OCTAVE Induction 1, OCTAVE Induction 2 and OCTAVE Sustain – which demonstrated that statistically significant and greater proportion of patients achieved remission when treated with Xeljanz compared to a placebo.
Pfizer is currently evaluating Xeljanz in an open label long-term extension study, OCTAVE Open.
However, there are several blockbuster drugs in the inflammatory segment approved for UC, which includes Johnson & Johnson’s (JNJ - Free Report) Remicade and Simponi, AbbVie’s (ABBV - Free Report) Humira and Shire’s Lialda. Moreover, many biotech companies are developing their candidates for the treatment for UC. Hence, competition is likely to increase in this segment.
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Pfizer's Arthritis Drug Gets FDA Nod for Ulcerative Colitis
Pfizer Inc. (PFE - Free Report) announced that the FDA has approved the label expansion of its JAK inhibitor, Xeljanz (tofacitinib), to include a new indication – moderately to severely active ulcerative colitis (“UC”). The drug is approved for the treatment of adult patients with recommended a dose of 10 mg twice-daily for at least eight weeks.
The approval was expected as the FDA Gastrointestinal Drugs Advisory Committee had adopted a positive vote in a meeting in March recommending the approval of the supplemental new drug application (sNDA) filed in July last year seeking label expansion of Xeljanz in UC.
Xeljanz is already marketed for the treatment of rheumatoid arthritis and active psoriatic arthritis. In the first quarter of 2018, Xeljanz sales were $326 million, up 30.4% from the year-ago period. The label expansion in the UC indication is likely to boost its sales further.
Shares of Pfizer have lost 0.5% so far this year, compared with a 6% decrease for the industry it belongs to.
The approval was based on data from three pivotal studies – OCTAVE Induction 1, OCTAVE Induction 2 and OCTAVE Sustain – which demonstrated that statistically significant and greater proportion of patients achieved remission when treated with Xeljanz compared to a placebo.
Pfizer is currently evaluating Xeljanz in an open label long-term extension study, OCTAVE Open.
However, there are several blockbuster drugs in the inflammatory segment approved for UC, which includes Johnson & Johnson’s (JNJ - Free Report) Remicade and Simponi, AbbVie’s (ABBV - Free Report) Humira and Shire’s Lialda. Moreover, many biotech companies are developing their candidates for the treatment for UC. Hence, competition is likely to increase in this segment.
Pfizer Inc. Price
Pfizer Inc. Price | Pfizer Inc. Quote
Pfizer currently has a Zacks Rank #3 (Hold). You can see the complete list of today’s Zacks #1 Rank (Strong Buy) stocks here.
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Here's another stock idea to consider. Much like petroleum 150 years ago, lithium power may soon shake the world, creating millionaires and reshaping geo-politics. Soon electric vehicles (EVs) may be cheaper than gas guzzlers. Some are already reaching 265 miles on a single charge.
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