Onesource Specialty Pharma Limited (NSE: ONESOURCE) announced its consolidated financial results for the quarter ended September 30, 2026, showcasing robust performance with revenue up 37% year-over-year and EBITDA up 53% year-over-year. The company reported revenue of ₹5,162 million, a 37% increase compared to the same quarter last year, and an EBITDA of ₹1,633 million, marking a 53% rise year-over-year. These impressive figures highlight the company’s strong operational leverage and strategic growth initiatives.

Revenue and EBITDA Growth

The revenue of ₹5,162 million reflects a 37% year-over-year increase and a 15% quarter-over-quarter increase. This growth is driven by the new DDC (drug-device combination) capacity, robust MSA (Master Service Agreement) execution, and multiple product launches across all business segments. The EBITDA of ₹1,633 million shows a 53% year-over-year increase and a 32% quarter-over-quarter increase, with margins expanding to 32%, driven by operating leverage from higher volumes across the business.

Adjusted PAT and EPS

The adjusted PAT stood at ₹937 million, with an adjusted EPS of ₹8.2, showing a 109% year-over-year increase. This significant growth is supported by the company’s strategic initiatives and operational efficiencies. The adjusted figures exclude exceptional items and scheme-related intangible amortization.

Mr. Neeraj Sharma, CEO & MD of OneSource Specialty Pharma Limited, commented, “Q2 delivered strong sequential growth, led by new DDC capacity. With our second cartridge line commercial, H2 will see new launches and a significant ramp-up in commercial volumes. Biologics momentum remained strong, with yet another US biotech onboarded during the quarter. With additional capacity and partnerships, we are well set for the next phase of growth.”

Source: NSE Corporate Announcement

Fundamental & Technical Analysis of Onesource Specialty Pharma Limited

Onesource Specialty Pharma Limited belongs to the Healthcare › Biotechnology sector. Here’s a quick read on where the business and the stock stand today.

Onesource falls 14.8% over three months and has not found a floor yet. Razor-thin margins below 5% make profitability extremely vulnerable — this business needs scale or pricing power urgently. No meaningful dividend — total return is entirely dependent on capital appreciation. RSI stands at 30, well into oversold territory. Yet sellers still dominated on 17 of recent sessions versus 13 for buyers, so the pressure has not fully lifted. Revenue grows at 232.4% yet the PEG reaches 99.00 — expensive for that growth. Furthermore, the stock drops 14.8% in three months. Neither value nor momentum supports this setup. It needs an earnings beat or a price reset first. Check Fundamentals of Onesource Specialty Pharma Limited.

Biocon Limited (NSE: BIOCON) announced that its Pertuzumab biosimilar has become the first biosimilar to secure a positive opinion from the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA). This approval recommendation under the new tailored clinical approach marks a significant milestone for Biocon Biologics Limited, a wholly-owned subsidiary of Biocon Limited. The biosimilar, marketed under the brand name Pebrilzo®, is indicated for the treatment of HER2-positive breast cancer across multiple disease stages.

Extensive Clinical and Analytical Validation

The positive CHMP opinion follows a comprehensive review of the marketing authorization application submitted by Biocon Biologics Ireland Limited. Extensive orthogonal, state-of-the-art structural and functional analytical characterization, together with comparative clinical pharmacokinetic data, demonstrated that Pebrilzo® is highly similar to the reference biologic, with no clinically meaningful differences in quality, safety, or efficacy.

Expanding Access to Biologic Therapies

Shreehas Tambe, CEO & Managing Director of Biocon, said: “The positive CHMP opinion for our Pertuzumab biosimilar marks an important step toward expanding access to biologic therapies for patients with HER2-positive breast cancer in Europe.” This approval reflects an important milestone in the evolution of biosimilar science and greater regulatory confidence on advanced analytical and clinical pharmacology evidence to establish biosimilarity.

As the first monoclonal antibody biosimilar to receive a positive CHMP opinion under EMA’s tailored clinical development approach, this approval is a testament to Biocon’s commitment to providing affordable, life-changing medicines to patients worldwide.

Source: NSE Corporate Announcement

Fundamental & Technical Analysis of Biocon Limited

Biocon Limited belongs to the Healthcare › Biotechnology sector. Here’s a quick read on where the business and the stock stand today.

Biocon moves sideways over three months, with neither buyers nor sellers taking control. Razor-thin margins below 5% make profitability extremely vulnerable — this business needs scale or pricing power urgently. Revenue consistency is the one bright spot — zero dips in five years shows operational resilience. The stock holds at 44% of its 52-week range with RSI at 35. In other words, neither side has a clear edge right now. Revenue grows at 15.3% and the stock moves sideways over three months. Neither side makes a strong case. The next earnings print will likely break this stock out of its current range. Check Fundamentals of Biocon Limited.

Biocon Limited (NSE: BIOCON) has announced the signing of a 10-year supply contract for Pertuzumab in Brazil, marking a significant milestone in advancing HER2-positive breast cancer therapy. The contract was signed with Bahiafarma and Bionovis, under Brazil’s Productive Development Partnership (PDP) program. The consortium received 100% allocation under Brazil’s 10-year PDP program for Pertuzumab, providing exclusive access to Brazil’s public healthcare market.

Strategic Partnership

Shreehas Tambe, CEO & Managing Director of Biocon, emphasized the transformative potential of strong partnerships in building local capabilities and expanding access to affordable medicines. This contract enables Biocon to reach more patients with HER2-positive breast cancer and address an important healthcare need at scale.

Market Impact

The PDP framework supports the long-term adoption of Biocon’s product within Brazil’s public oncology network. The product will undergo phased localization in Brazil in the mid to long term, ensuring sustainable access to this important cancer therapy. This partnership also contributes to Brazil strengthening its capacity to produce essential medicines for its Unified Health System (SUS).

Future Prospects

As part of the PDP, Biocon will receive milestone payments and a share of revenues generated from the Brazil PDP opportunity over a 10-year period. This agreement not only supports better patient outcomes but also helps build a stronger, more resilient healthcare ecosystem in Brazil.

Source: NSE Corporate Announcement

Fundamental & Technical Analysis of Biocon Limited

Biocon Limited belongs to the Healthcare › Biotechnology sector. Here’s a quick read on where the business and the stock stand today.

Biocon moves sideways over three months, with neither buyers nor sellers taking control. Razor-thin margins below 5% make profitability extremely vulnerable — this business needs scale or pricing power urgently. Revenue consistency is the one bright spot — zero dips in five years shows operational resilience. RSI stands at 28, well into oversold territory. Yet sellers still dominated on 18 of recent sessions versus 12 for buyers, so the pressure has not fully lifted. Revenue grows at 15.3% and the stock moves sideways over three months. Neither side makes a strong case. The next earnings print will likely break this stock out of its current range. Check Fundamentals of Biocon Limited.