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Glenmark Pharmaceuticals Ltd. is looking to double its revenue growth in the next four years.
To maximise shareholders’ wealth, the company aims to attain zero net debt and earn a 22% return on capital employed in the next four to five years amid a continuous improvement in Ebitda margin, it said in its exchange filing.
The pharmaceutical company intends to accomplish this by increasing its share of the branded generics business, controlling R&D spending, and improving operating leverage, according to a Nov. 17 investor meeting.
The Mumbai-based drugmaker is also evaluating enhancing dividend pay-outs and share buybacks over the next four years. Despite this, share prices declined a day after the announcement.
Shares of the company declined 3.95% to Rs 412.35 apiece as of 12:40 p.m., while the benchmark Nifty 50 eased 0.54% on the NSE. It had hit an intraday low of Rs 408.50 apiece, a day after the investors’ meeting.
The brokerage maintained a ‘neutral’ ratings, with a target price of Rs 420 apiece, implying a downside of 2%.
ROCE Boost
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Aims to boost ROCE (EBIT/capital employed) to 22% by FY27 from 17% in FY22.
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This will be done by increasing the share of business from branded generics, keeping R&D costs for the new chemical entity portfolio under control, and improving operating leverage.
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Focusing on core therapies like dermatology, respiratory, cardiac, and anti-diabetes will help improve existing brand franchises.
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4-5% of growth in domestic formulation to be led by launches.
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To further monetise the brands, the company is working to transition from prescription generics to over-the-counter products.
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The company expects 6% annualised sales over FY22-24.
Filings update
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The benefit from complex product filings is expected from FY25 but is subject to timely approval.
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Glenmark Pharma has 46 ANDAs that are waiting to be approved. It is also working on eight to 10 injectables, two to three drug-device combinations, and three to four generics for the respiratory portfolio.
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The near-term target is to complete the proof-of-concept study for ISB1342 and ISB1442 before March 2023. The successful clinical trials will enable it to launch in CY26 and CY27, respectively.
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It also intends to close one oncology partnership before the end of FY23.
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It plans to file an investigational new drug for ISB2001 before March 2023.
Update on regulatory issues
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Asset utilisation at Monroe for the US market is subject to the successful resolution of regulatory issues, which are under ‘official action initiated’ status.
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Injectable commercialisation is hinged on successful compliance at Monroe.
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There is also an import alert issued to its Baddi facility by the U.S. FDA.
Other highlights
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The management aims to attain zero net debt by FY26.
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It intends to achieve 10-12% annualised sales growth over the next four years.
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Reduce R&D spends to 8.5-9% of sales from FY24 versus 10.4% in H1FY23.
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Aims to scale up revenue from Ryaltris [nasal spray] to $100-150 million [around Rs 817-1,226 crore] by FY27 from $30 million [Rs 245 crore] in FY22.
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The company expects to maximise business prospects in Europe through an in-house pipeline as well as strategic in-licensing, given 11% of the total revenues in the second quarter were from Europe.
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The brokerage anticipates that the European market will grow at an annualised rate of 11% between FY22 and FY24.
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Management expects the company to grow and gain market share in the rest of the world through in- and out-licensing of key product.
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