Glenmark Pharma reports revenue growth of 11.7% YoY Q4; 5.6% for the full year FY 2022-23
Glenmark Pharmaceuticals Limited (Glenmark), an innovation-driven global pharmaceutical company, today announced its financial results for the fourth quarter ended March 31, 2023.
For the fourth quarter of FY 2022?23, Glenmark’s consolidated revenue was at 33,737 Mn as against 30,191 Mn recording an increase of 11.7% YoY.
EBITDA was 6,050 Mn in the quarter ended March 31, 2023, as compared to 4,634 Mn in the previous corresponding quarter, registering growth of 30.5%. EBITDA margin for Q4 FY 2022-23 was 17.9 %.
Reported net loss 4,031 Mn for the quarter ended March 31, 2023 on account of an exceptional loss of 7,997 Mn 2 , primarily on account of settlement of the litigation related to generic Zetia® in the U.S.
For the year ended March 31, 2023, Glenmark’s consolidated revenue was at 1,29,901 Mn as against 123,049 Mn, recording an increase of 5.6 % over the previous corresponding period.
EBITDA for the fiscal year ended March 31, 2023 stood at 22,784 Mn as against 23,203 Mn in the previous corresponding period. EBITDA margin for FY 2022-23 was at 17.5%.
Net Profit (PAT) 3 was at 3,774 Mn for the year ended March 31, 2023, as against 9,936 Mn in the previous year. The PAT 3 for FY 2022-23 was lower on account of exceptional loss of 7,659 Mn 2 primarily on account of settlement of the litigation related to generic Zetia® in the U.S.
“We delivered yet another year of robust performance, despite the challenging global macro-economic environment. Our India business recorded double-digit growth in secondary sales. The North America business showed strong recovery, and the EU and RoW markets did phenomenally well. We continued to make headway in launching Ryaltris®, our first global branded specialty product. Additionally we initiated the Proof-of-Concept studies for four of our clinical oncology assets, which are part of the Glenmark/Ichnos pipeline,” said Glenn Saldanha, Chairman and Managing Director, Glenmark Pharmaceuticals Ltd. He further added, “We look forward to continue this momentum in the coming year with double-digit revenue growth and significant improvement in EBITDA margins.”
GLENMARK PHARMACEUTICALS LTD.
Sales from the India formulation business for the fourth quarter of FY 2022-23 were at 8,284 Mn as against 8,847 Mn in the previous corresponding quarter, recording decline of 6.4%.
North America registered revenues of 8,507 Mn in Q4 FY2022-23; recording growth of 15.3%, as against revenue of 7,378 Mn for Q4 FY2021-22.
Asia, MEA, LATAM and RCIS Region (RoW)
For the fourth quarter of FY 2022-23, revenues from the RoW region were 6,856 Mn as against 5,479 Mn for the previous corresponding quarter, recording growth of 25.1%.
Glenmark Europe operations revenues for Q4 FY 2022-23 were at 6,078 Mn as against 4,968 Mn, recording growth of 22.3%.
Respiratory – Creating a global scale
As of the end of the fourth quarter of FY 2022-23, marketing applications for Ryaltris® have been submitted in more than 70 countries across the world. The product has been commercialized in 27 markets, including major markets like the USA, Europe (the UK and multiple markets across the EU), Australia, Russia, South Africa, and South Korea.
Other key products
- Clinical trial ongoing for generic Flovent pMDI; expect to file in FY24.
- Plan to file at least one more generic respiratory pMDI in the U.S. in FY24 and continue filing momentum beyond FY24
Innovative R&D Pipeline
GRC 54276 (HPK1 Inhibitor) is being developed as a novel, orally administered immunotherapeutic agent for patients with solid tumors. Hematopoietic progenitor kinase 1 (HPK1) is a negative regulator of T and B cell receptor signaling, and an attractive therapeutic strategy for immuno-oncology based treatment in cancers. In pre-clinical studies, GRC 54276, when administered alone, has demonstrated substantial anti-tumor effects. These are further enhanced when administered in combination with currently available immunotherapy.
GRC 54276 is currently being evaluated in the First in Human (FIH) phase 1 clinical study (GRC 54276-101). Part 1a monotherapy phase of the study is ongoing in India since July 2022 and no dose-limiting toxicities have been observed during the DLT period to-date. U.S. FDA’s acceptance of the IND was received in Q4 FY 2022-23. Initiation of the Part1b of the study for GRC 54276 in combination with pembrolizumab and atezolizumab in India and the U.S. is planned for Q1 FY24.
GRC 39815 (RORγt inhibitor) is the company’s respiratory pipeline asset being developed as an inhaled therapy for treatment of mild-to-moderate Chronic Obstructive Pulmonary Disorder (COPD). It is currently under Phase 1 clinical development in the U.S.
GLENMARK LIFE SCIENCES LTD. (GLS)
Revenues from operations, including captive sales, were 6,213 Mn as against 5,141 Mn, recording a YoY growth of 21%. Generic API revenues in Q4 FY 2022-23 increased by 10.4% QoQ and increased by 15.5% YoY. The business witnessed steady growth momentum across regulated as well as emerging markets. CDMO revenues in Q4 FY 2022-23 doubled sequentially and grew by 30.4% YoY in Q4 FY 2022-23. DMF/CEPs filing continued across major markets in Q4 FY 2022-23; taking the total cumulative filings to 468 as on March 31, 2023. Multiple projects are completed / ongoing for capacity expansion across the Ankleshwar and Dahej facilities.
External sales for GLS in Q4 FY 2022-23 were at 3,831 Mn as against 3,283 Mn in Q4 FY 2021-22; recording a growth of 16.7% YoY.
ICHNOS Sciences (Ichnos)
For the fourth quarter of the current financial year, Glenmark invested 1,906 Mn as compared to 1,640 Mn in the previous corresponding quarter. For the twelve months of FY 2022-23, Glenmark has invested 6,833 Mn as compared to 6,627 Mn in the corresponding period of the previous financial year.
Source : Press Release
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