Theranica Secures $45 Million Series C Funding Round

Theranica, a prescribed digital therapeutics company developing advanced neuromodulation devices for migraine and other idiopathic pain conditions, today announced the closing of its Series C funding round, with a first closing of $45 million.

Philadelphia-based New Rhein Healthcare Investors led the round, with wide participation of existing investors aMoon, Lightspeed Venture Partners, LionBird, Takoa Invest, and Corundum Open Innovation. Due to high investor interest, the company has extended the financing round, planning a final closing in October. Proceeds of the new funds will focus on expanding the company’s commercial activity in the U.S.

“In spite of several decades of new medications, millions of individuals still suffer from frequent debilitating migraine headaches,” said Alon Ironi, CEO of Theranica. “Over the last couple of years, we have verified the three fundamental conditions of a successful new prescribed therapy in the U.S.: healthcare providers have confidence in prescribing our Nerivio for treating migraine, patients get significant clinical benefit from using it, and Payors realize the importance of providing their insured members with access to this therapy. With this triad demonstrated, we needed the appropriate funding to unleash the huge potential of Nerivio in the U.S.”

Ironi added, “New Rhein’s investment team is a group of seasoned pharma executives with vast international experience in the clinical and business aspects of the healthcare domain. Having them on the team is a powerful multiplier in our journey to bring effective, drug-free therapeutic options to millions of people with migraine, and in the future to millions of people with other chronic pain diseases.”

Nerivio is an FDA-cleared, prescribed, smartphone-controlled, drug-free wearable device for the treatment of episodic and chronic migraine in people aged 12 and older. Uniquely worn on the upper arm at the onset of a migraine attack, Nerivio alleviates migraine headache and associated symptoms by utilizing remote electrical neuromodulation to trigger an endogenous analgesic mechanism, known as conditioned pain modulation.

Dr. Greg Parekh, Founder and Managing Partner at New Rhein Healthcare Investors said, “A sequence of recent discoveries in neuroscience is driving a paradigm shift in the treatment of neurological diseases. We believe Nerivio represents the first major breakthrough for the non-pharmacological treatment of migraine headaches. We spent a year exploring this market and its participants prior to choosing to invest into Theranica and believe the migraine medical community and patients are at a critical inflection point in their understanding of the benefits of Nerivio. With our pharma backgrounds, we were highly impressed with Theranica’s clinical data and user-friendly product design. We look forward to supporting the company in its commercial expansion.”

Multiple clinical trials, and several real-world evidence studies with thousands of patients, have shown Nerivio to be comparable to standard of care pharmacological options and able to be used as a standalone treatment or in combination with existing treatments. Eligible for insurance coverage and available to patients seeking cost-effective drug-free therapies for migraine, Nerivio can be prescribed by any certified healthcare provider in the U.S. and is shipped to patients’ homes through several specialty pharmacies.

“More than half of the 40 million Americans who live with migraines are unsatisfied with their current treatments. We are encouraged by the amazing feedback we have received from the tens of thousands of patients already using Nerivio and are determined to make Nerivio a first-line therapy,” said Dr. Shimon Eckhouse, Chairman and Co-Founder of Theranica. “We are pleased to have New Rhein join Theranica as the lead investor of round C and as a partner that will play a key role in building and maximizing the value of the company. Theranica’s excellent clinical data and positive feedback from both patients and providers, combined with our strong financial position, will enable us to bring our solutions to millions of patients in the U.S. and worldwide.”

SourceTheranica

Hot this week

Spartan Medical Broadens Single-Use Sterile Instrument Portfolio to Improve Outcomes, Increase Efficiency, and Generate Cost Savings

Spartan Medical products portfolio of single-use, sterile med tech includes micro and minor surgical convenience kits, kerrison rongeurs, spinal and general surgical retractors, dural repair kits, synthetic biologics, and a wide range of orthopedic pre-sterilized implants and devices.

Recor Medical Supports European Society of Cardiology’s Hypertension Guidelines

Record Medical notes the new guidelines, "2024 ESC Guidelines for the management of elevated blood pressure and hypertension," have been published online and recommend the consideration of renal denervation (RDN) as a safe and effective treatment option for patients who have uncontrolled resistant hypertension or those that have uncontrolled hypertension with a higher risk of cardiovascular disease, who express a preference to undergo RDN.

ConTIPI Medical Selects EVERSANA to Support U.S. Commercialization of Non-Surgical Medical Device ProVate for Women with Pelvic Organ Prolapse

EVERSANA is a leading provider of global commercial services to the life sciences industry, to support commercialization for the ProVate device in the United States to help women experiencing pelvic organ prolapse.

Boston Scientific Obtains CE Mark for ACURATE Prime Aortic Valve System

The ACURATE Prime aortic valve system is designed with several features to build upon the clinical performance of the ACURATE neo2™ platform including an additional valve size, which expands the treatment range to patients with a larger anatomy.

Noctrix Health Announces New CMS Reimbursement Codes and Payment for Nidra Tonic Motor Activation Therapy for Restless Legs Syndrome

Nidra TOMAC Tonic Motor Activation Therapy, which was authorized for marketing in the United States last year following its designation as a "Breakthrough Device" by the US Food & Drug Administration (FDA), remains the only clinically validated, non-pharmaceutical treatment available for patients with RLS.