-

Kashiv BioSciences and CRISTÁLIA Enter into Licensing and Supply Agreement for Omalizumab Biosimilar (ADL-018) in Latin America

PISCATAWAY, N.J.--(BUSINESS WIRE)--Kashiv BioSciences, LLC (“Kashiv” or the “Company”) today announced that it has entered into a licensing and supply agreement with CRISTÁLIA, one of the leading pharmaceutical companies in Brazil, for the commercialization of ADL-018 / bOmalizumab, a proposed biosimilar to Xolair®, in Latin America (LATAM). In 2024, IQVIA recorded approximately $5.0 billion in global sales, with approximately $140 million contributed by the LATAM region.

Dr. Sandeep Athalye, Chief Executive Officer at Kashiv BioSciences said, “CRISTÁLIA is an ideal partner to commercialize ADL-018 across Latin America, supporting Kashiv’s mission to expand its biosimilar portfolio and increase global access."

Share

Under the terms of the agreement, Kashiv BioSciences is responsible for the development of the product within the agreed territories. CRISTÁLIA will be responsible for the licensing, distribution, and commercialization of ADL-018 in the LATAM region.

Dr. Sandeep Athalye, Chief Executive Officer at Kashiv BioSciences said, “CRISTÁLIA is an ideal partner to commercialize ADL-018 across Latin America, supporting Kashiv’s mission to expand its biosimilar portfolio and increase global access. We look forward to CRISTÁLIA bringing our omalizumab biosimilar to patients in this important region.”

“We are thrilled to have entered a partnership with Kashiv for the licensing of Omalizumab biosimilars in the LATAM region,” Dr. Ogari Castro Pacheco, Chairman of CRISTÁLIA stated, “CRISTÁLIA is confident that this molecule will be a key asset to our biosimilars portfolio and as part of our company strategy to expand patient access to high quality, affordable treatments in the future.”

About ADL-018:

ADL-018 is a proposed Xolair® biosimilar. Omalizumab is a humanized monoclonal antibody that targets free immunoglobulinE (IgE). Xolair® is indicated for the treatment of Chronic Idiopathic Urticaria (CIU) or Chronic Spontaneous Urticaria (CSU), severe persistent allergic asthma, chronic rhinosinusitis with nasal polyps (CRSwNP), and IgE-mediated food allergy. ADL-018 is an investigational product and has not received regulatory approval in any country. Biosimilarity has not been established by regulatory authorities and is not claimed.

Xolair® is a registered trademark of Genentech, Inc. and Novartis AG.

About Kashiv BioSciences

Kashiv BioSciences, LLC is a vertically integrated biopharmaceutical company with numerous commercial and advanced clinical-stage assets and is among the few U.S.-based companies to both manufacture and receive marketing authorization for multiple biosimilars. Kashiv BioSciences, LLC in the USA, and its subsidiaries in India (together “Kashiv BioSciences”) operate together with a robust infrastructure and highly skilled teams that provide global R&D, clinical, manufacturing, regulatory, and IP capabilities. We believe our people, partners, and shared purpose fuel our work to advance patient care and access to important medicines.

For more information, please visit https://www.kashivbiosciences.com/

About CRISTÁLIA

CRISTÁLIA is a private owned Brazilian biopharma company, with 53 years of operation and a broad footprint across the main Latin America markets. CRISTÁLIA is dedicated to the discovery, development, manufacturing, and commercialization of life-saving treatments to patients with severe, life-threatening diseases or injuries.

In addition to the biopharmaceutical business, CRISTÁLIA also ranks between the biggest API manufacturers in Latin America, with state-of-the-art facilities dedicated to the manufacturing of synthetic, oncologic and biotech active ingredients.

CRISTÁLIA is headquartered in Campinas (Brazil).

For more information, please visit Cristália - Indústria Farmacêutica

Contacts

Media Contact Kashiv BioSciences

Dr. Paras Vasanani

Global Head of Business Development, Portfolio & Strategy

paras.vasanani@kashivbio.com

Media Contact CRISTÁLIA

Marina Prata

Director Corporate Marketing

marina.prata@cristalia.com.br

Kashiv BioSciences, LLC


Release Versions

Contacts

Media Contact Kashiv BioSciences

Dr. Paras Vasanani

Global Head of Business Development, Portfolio & Strategy

paras.vasanani@kashivbio.com

Media Contact CRISTÁLIA

Marina Prata

Director Corporate Marketing

marina.prata@cristalia.com.br

More News From Kashiv BioSciences, LLC

Kashiv Biosciences Announces Submission of Biologics License Application to U.S. FDA and Acceptance of Market Authorization Application by European Medicines Agency for ADL-018, a Proposed Biosimilar to XOLAIR® (omalizumab)

PISCATAWAY, N.J.--(BUSINESS WIRE)--Kashiv BioSciences, LLC, a fully-integrated biopharmaceutical company, announced that they have submitted a Biologics License Application (BLA) to the U.S. Food and Drug Administration (FDA), and the European Medicines Agency (EMA) has accepted the Marketing Authorization Application (MAA), for ADL-018, a proposed biosimilar to XOLAIR® (omalizumab). The submissions are intended to seek approval in the United States and the European Economic Area, respectively....

Kashiv BioSciences and JAMP Pharma Corporation Announce the Launch of PEXEGRA® and FILRA® Biosimilars in Canada

PISCATAWAY, N.J.--(BUSINESS WIRE)--Kashiv BioSciences, LLC today announced the commercial launch of PEXEGRA®, a biosimilar referencing Neulasta®, and FILRA®, a biosimilar referencing Neupogen®, in the Canadian market. Both biosimilars will be marketed in Canada through an exclusive agreement with JAMP Pharma Corporation. PEXEGRA® (6 mg/0.6 mL pre-filled syringe) and FILRA® (300 mcg/0.5 mL and 480 mcg/0.8 mL pre-filled syringe) are used to treat neutropenia, low neutrophils which are a type of w...

Kashiv BioSciences and MS Pharma Enter into MENA License and Supply Agreement for ADL-018, Biosimilar Candidate to XOLAIR® (bOmalizumab)

PISCATAWAY, N.J.--(BUSINESS WIRE)--Kashiv BioSciences, LLC and MS Pharma today announced that the companies have entered into a license and supply agreement for ADL-018, Kashiv BioSciences’ biosimilar candidate to XOLAIR® (bOmalizumab) in the Middle East and North Africa (MENA) region. IQVIA reported global sales of ~$4.5 billion and ~$60 million in MENA in 2024. Under the terms of the agreement, Kashiv BioSciences is responsible for the development of the product within the agreed territories....
Back to Newsroom