Profit up on new compound; big plans for SUVN-502: Suven

Written By Unknown on Selasa, 12 Februari 2013 | 18.00

Venkat Jasti, CEO of Suven Life Sciences says the drug manufacturer's profit in the third quarter jumped by 500 percent to Rs 7.7 crore due to the supply of a value-added compound, by the company's contract-research arm.

Going forward, Jasti says, the company was preparing to fast-track the development of its Alzheimer drug candidate SUVN-502. "We are in the final stages of putting a development team in place," he told CNBC-TV18 in an interview.

Below is the edited transcript of the interview on CNBC-TV18

Q: What is your revenue, EBITDA and profitability this quarter?

A: Our revenue growth was about 25 percent this quarter and the growth in profits-after-tax (PAT) was about 500 percent. Revenue increased from 50 crore to Rs 63 crore and profit was Rs 7.75 crore versus Rs 1.3 crore.

Q: What has led to this strong jump in your profitability this quarter?

A: Our contract research business supplied a value-added compound during this quarter.

Q: Did you receive any milestone payments this quarter?

A: No, the payments were not a milestone category. The payment is according to a supply agreement.

Q: Will you begin to supply any active pharmaceutical ingredients (API) drugs because of this?

A: This is not an API. This is an Advanced Intermediate and it will be certainly long-term because we can supply this when it is marketed hopefully, next year. My customer will be putting a new drug application (NDA) and based on that our volumes will also go up from next year onwards.

Q: What was research and development (R&D) costs this quarter and how much did it comprise of in terms of a percentage of revenues?

A: The percentage of R&D costs to revenue is about 15 percent, about Rs 8 crore this quarter.

Q: What are your operating margins EBITDA?

A: The EBITDA is Rs 13 crore and operating margins are about 24 percent.

Q: You have ten patents from Canada and 12 from Eurasia. What is the development on the new chemical entities (NCEs) at this point in time?

A: We are preparing to put SUVN-502 on a fasttrack mode into phase II-A clinical trials and we have almost finalised a protocol. There are two small-bridge studies to be conducted before we file the investigational new drug (IND) in the USA. We are in the final stages of putting a development team in place within the next two-to-three months.

Q: Any licensing deals we can expect going into 2013?

A: As of now, there are no deals in the pipeline.



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