FDA Accepts Filing of New Estrogen-free Oral Contraceptive

Exeltis has received acceptance from the US Food and Drug Administration (FDA) of the filing of Slinda (4mg Drospirenone-only pill), the novel oral contraceptive developed by the company. The Prescription Drug User Fee Act (PDUFA) date is expected during the 27 May of 2019.

Slinda is an investigational estrogen-free oral contraceptive, with a 24/4 dose regimen that is believed to have a favorable safety and efficacy profile.

"Developed by Exeltis, part of the global pharmaceutical group Insud Pharma, Slinda showed to be safe, efficacious and well tolerated during extensive clinical trials. Once available in the market, it could give an improved bleeding profile and greater flexibility, maintaining contraception efficacy for up to 24 hours in the event of a delayed or missed pill dosage," said Yann Brun, Managing Director Exeltis.

Drospirenone is a synthetic progestin with a pharmacological profile similar to natural-produced progesterone. As an estrogen-free contraceptive option, Slinda is expected to reduce the cardiovascular risks associated with Combined Hormonal Contraceptives (CHCs) and to offer all the unique advantages of drospirenone in terms of safety and tolerability and antimineralocorticoid and antiandrogenic activity.

"We are delighted that Slinda brings us one step closer to providing women in the United States with a new effective, safe and well-tolerated method of contraception," said Salustiano Perez, President Exeltis USA.

The submission of Slinda is based on an extensive development program involving more than 3,000 patients, generating over 20,000 cycles. The study showed that Drospirenone 4 mg-only pill has a clinical efficacy historically comparable to CHCs.

"No cases of thromboembolic events were reported in the entire clinical program. The safety profile was demonstrated for all women, even higher-risk population segments, such as smokers, over-35s and obese patients," said Enrico Colli, MD, Chief Scientific Officer.

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