Liferna’s integrated global partner network is designed to accelerate development, expand access, and support long-term commercialization success. Through strategic collaborations with innovators including Bio-Thera Solutions and University of Michigan, together with leading contract research, manufacturing, and supply partners (CRO, CMO, and CSO partners), we bring together scientific expertise, clinical execution, manufacturing excellence, and commercialization capabilities to advance life-changing medicines globally.
Our collaboration model extends beyond development to include regional clinical development support, clinical and commercial supply capabilities for emerging and advanced markets, and a scalable manufacturing strategy designed to strengthen supply continuity and support future global demand. United by a shared commitment to patients, we work across disciplines and geographies to accelerate access to transformative medicines worldwide.
Advancing transformative therapies across oncology, autoimmune, and fibrotic diseases, with the goal of delivering meaningful breakthroughs for patients.
LFR-1101 LFR-1101 is an investigational humanized anti-PD-1 monoclonal antibody being evaluated for treatment of multiple cancers, including cervical cancer.
Cervical cancer is a serious gynecologic malignancy often associated with persistent human papillomavirus (HPV) infection. While current treatment options can provide benefit, patients with advanced or recurrent disease continue to face significant unmet medical needs, highlighting the importance of developing new immunotherapy approaches designed to enhance anti-tumor immune responses.
LFR-1201 LFR-1201 is an investigational small molecule therapy being developed through the U.S. FDA’s 505(b)(2) regulatory pathway for the treatment of idiopathic pulmonary fibrosis (IPF).
Idiopathic pulmonary fibrosis is a chronic, progressive lung disease characterized by the formation of scar tissue within the lungs. As the disease advances, lung function declines, making it increasingly difficult for patients to breathe and perform everyday activities. IPF is associated with substantial morbidity and mortality, and despite available treatments, many patients continue to experience disease progression. Additional therapeutic options are needed to help address the underlying fibrotic process and improve outcomes for individuals living with IPF.
LFR-1201 LFR-1201 is an investigational small molecule therapy being developed through the U.S. FDA’s 505(b)(2) regulatory pathway for patients with systemic sclerosis (SSc).
Systemic sclerosis is a rare chronic autoimmune disease characterized by progressive fibrosis of the skin and internal organs, as well as abnormalities of the blood vessels and immune system. Patients may experience skin thickening, pain, fatigue, reduced mobility, and potentially serious organ involvement that can significantly impact quality of life. Despite available treatment approaches that help manage symptoms and complications, there remains a need for additional therapies that address the underlying disease process and improve outcomes for individuals living with systemic sclerosis.
LFR-1501
Charcot-Marie-Tooth Disease Type 1 (CMT-1)
LFR-1501 LFR-1501 is an investigational neural regenerative progenitor cell (NRPC) therapy being evaluated for the treatment of Charcot-Marie-Tooth Disease Type 1 (CMT-1).
Charcot-Marie-Tooth Disease Type 1 is a rare inherited neurological disorder that affects the peripheral nerves responsible for muscle movement and sensation. The disease typically causes progressive muscle weakness, sensory loss, balance difficulties, and impaired mobility, which can significantly impact daily activities and quality of life. While supportive therapies may help manage symptoms, there are currently limited treatment options that address the underlying disease process. New therapeutic approaches are needed to help preserve nerve function and improve outcomes for individuals living with CMT-1.
LFR-1501
Diabetic Neuropathy (DN)
LFR-1501 LFR-1501 is an investigational neural regenerative progenitor cell (NRPC) therapy being evaluated for the treatment of diabetic neuropathy (DN).
Diabetic neuropathy is one of the most common complications of diabetes, resulting from progressive nerve damage associated with chronically elevated blood glucose levels. Patients may experience numbness, tingling, pain, weakness, and loss of sensation, particularly in the feet and lower extremities, which can significantly affect mobility, independence, and quality of life. While currently available treatments may help manage symptoms, additional therapeutic options are needed to address the underlying nerve damage and improve outcomes for individuals living with diabetic neuropathy.
LFR-1502
Osteoarthritis (OA)
LFR-1502 LFR-1502 is an investigational mesenchymal stem/stromal cell (MSSC) therapy being evaluated for the treatment of osteoarthritis (OA).
Osteoarthritis is the most common form of arthritis and a leading cause of pain, stiffness, and reduced mobility worldwide. The disease is characterized by the progressive degeneration of joint tissues, which can impair physical function and significantly impact quality of life. While currently available treatments may help manage symptoms, many patients continue to experience disease progression and functional decline. Additional therapeutic options are needed to help address the underlying disease process and improve outcomes for individuals living with osteoarthritis.
