GERMANTOWN, Md., June 16, 2023 (Newswire.com)
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Seraxis today announced late-breaking results of an ongoing study evaluating the efficacy of SRE pancreat…

New Virtual Mental Health and Substance Use (MHSU) Program From Compass Health Center Delivers Specialized Care to a Broader Audience, Bridging the Gap in Access to Essential Services

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KANSAS CITY, Mo., June 15, 2023 (Newswire.com)
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Dr. Irfan Handoo, a leading expert in psychiatry and renowned provider of transcranial magnetic stimulation (TMS) and IV ketamine treatments, is excited to announce the relocation of his clinic to a new state-of-the-art facility. The clinic has recently signed a lease and will move into a spacious 4,000-square-foot location at 7011 West 121st Street, Suite 105, Overland Park, KS 66209, on Monday, June 19.

This move marks a significant milestone for Dr. Handoo and his team as they continue their commitment to providing exceptional care and expanding access to cutting-edge treatments for patients struggling with mental health conditions. The new facility offers an environment designed to foster comfort and healing, providing a welcoming space for patients seeking TMS and IV ketamine treatments.

“We are thrilled to announce our upcoming move to Overland Park,” said Dr. Handoo. “This new clinic will allow us to serve our patients better, providing them with a modern and compassionate environment where they can continue to receive the high standards of care they have come to expect from us. Our goal is to create a nurturing space that complements the innovative treatments we offer, enabling our patients to find relief and improve their overall well-being.”

Deep TMS therapy, a noninvasive procedure that uses magnetic fields to stimulate targeted areas of the brain, has shown promising results in the treatment of treatment-resistant depression. IV ketamine treatments have also emerged as a breakthrough therapy for individuals who have not found relief from traditional treatments. Dr. Handoo’s expertise in administering these treatments, coupled with the new facility’s advanced capabilities, ensures that patients will receive the highest quality care in a comfortable and modern setting.

The new location boasts ample space for treatment rooms, cutting-edge equipment, and a welcoming reception area. Dr. Handoo and his team have meticulously designed the clinic to provide a serene and supportive atmosphere where patients can feel at ease throughout their treatment journey. The move to Overland Park represents a significant investment in the community and reaffirms Dr. Handoo’s commitment to improving mental health care in the region.

Patients seeking Deep TMS and IV ketamine treatments can schedule appointments at the new location starting Monday, June 19. Dr. Handoo and his team look forward to welcoming both existing and new patients to experience the enhanced care and comfort provided by the new clinic.

For more information about Dr. Irfan Handoo and his practice, please visit https://drhandoo.com/ or contact 816-441-9875.

Contact Information:

Dr. Irfan Handoo

[email protected]

816-441-9875

Original Source:

Kansas City’s Largest TMS and IV Ketamine Clinic Moving to Overland Park

Beginning in the second quarter of 2023, NIT will provide Actinium-225 in millicurie quantities, marking a significant step forward in cancer treatment

NIT Research Logo

DALLAS, June 15, 2023 (Newswire.com)
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Nano Imrad Technology (NIT), an innovative medical research and development company, is pleased to announce the availability of Actinium-225 for medical research and treatment. Beginning in the second quarter of 2023, NIT will provide Actinium-225 in millicurie quantities, marking a significant step forward in cancer treatment.

With the capacity to produce significant quantities of Actinium-225 daily, NIT is not only making this precious element more accessible, but is also contributing significantly to the global fight against cancer.

Actinium-225, a radioactive element, is gaining recognition in the medical community for its potential in targeted alpha therapy for cancer treatment. Its ability to deliver precise radiation directly to cancer cells, while leaving healthy tissue unaffected, has shown promise in shrinking and even eliminating tumors.

NIT has developed a breakthrough method to produce Actinium-225 in a reliable, safe, and cost-effective manner, overcoming traditional challenges associated with the production and acquisition of this element. This pioneering approach enhances access to Actinium-225, empowering researchers, clinicians, and patients to benefit from cutting-edge treatments and technologies.

NIT’s Actinium-225 will be available to licensed researchers, research institutions, and clinicians, who can utilize this crucial element for research and treatments. Actinium-225 is available only to organizations and individuals with a verified Radioactive Materials (RAM) License.

For more information about NIT and Actinium-225, please visit https://nitresearch.com.

About Nano Imrad Technology (NIT)

NIT is a medical research and development company specializing in the production of diagnostic imaging and therapeutic medical isotopes. Their core technology focuses on immune-labeled radionuclide nanoparticles, and their mission is to make Actinium-225 widely available for research and treatment purposes, revolutionizing the landscape of cancer treatment.

Contact Information:

Ed O’Connor

Director of Sales

[email protected]

+1 (332) 213-9516

Original Source:

Nano Imrad Technology (NIT) Announces Availability of Actinium-225, Pioneering a New Era of Cancer Treatment

Inspire Dental Wellness specializes in the non-surgical treatment of craniofacial pain to help patients improve their quality of life.

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DEXIS IOS Solutions is pleased to announce the expansion of its portfolio and ecosystem through new digital end-to-end workflows. Dental Practitioners can now easily expand their range of services through aligner and d…

Dr. Todd Lanman

SAN FRANCISCO, June 12, 2023 (Newswire.com)
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Todd Lanman, MD, of Lanman Spinal Neurosurgery and ADR Spinal Restoration Center, gave se…

The leading online ADHD treatment platform brings in Herman, who has more than two decades of managed care and pharmaceutical experience and is one of the leading experts in behavioral health.

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GAINESVILLE, Fla., June 12, 2023 (Newswire.com)
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Neobiosis, is a leading research and manufacturing biotechnology company focused on pioneering the development of novel therapeutics from perinatal tissues as a new class of medicines. Today, Neobiosis announced that the U.S. Food and Drug Administration (FDA) has approved the Investigational New Drug (IND) application for ViXome™, its drug for the treatment of ‘Post COVID Syndrome (AKA “Long Haul COVID Syndrome”).

“This is an important milestone for Neobiosis and we are excited to be advancing ViXome, a refined product extracted from thoroughly screened and sterile amniotic fluid obtained at the time of c-section of at-term pregnancies, into clinical development,” said Ian A. White, Ph.D., CEO and CSO of Neobiosis. “We are eager to confirm our preclinical data in the clinic and expect to begin enrolling patients in Phase 1 during the second quarter of 2024.”

ViXome, an acellular product derived from amniotic fluid, contains a heterogeneous population of growth factors, cytokines, chemokines, microRNAs and exosomes, which in pre-clinical testing has demonstrated potent immunomodulatory and pro-reparative effects.

The Phase I/IIa study will thoroughly investigate the safety and clinical efficacy of ViXome. Neobiosis products are processed in state-of-the-art, FDA-registered and FDA-inspected cGMP-compliant cleanrooms in Gainesville, FL. Neobiosis performs its research and development (R&D) at the University of Florida (UF) Sid Martin Innovate Biotechnology Institute in Alachua, FL., the world-recognized leader in biotechnology incubation.

“We are excited to be one of the first companies in the US to advance a potential therapeutic for the treatment of a devastating disease that already affects over 300 million people worldwide,” added Dr. White.

About Neobiosis 

Neobiosis is a clinical-stage biopharmaceutical company pioneering the development of perinatal tissue-derived therapeutics, a new class of medicines with the potential to transform the treatment of a wide spectrum of diseases with high unmet medical needs. By leveraging the biology of birth tissues as a natural source of regenerative and immunomodulatory cells, matrix and exosomes, Neobiosis has developed its proprietary platform to augment the innate properties of homeostasis to create a portfolio of novel therapeutic candidates. Neobiosis is dedicated to transparency, safety and efficacy of all of its products developed under FDA oversight.

Contact Information:

ian white

CEO

[email protected]

3059062345

Original Source:

Neobiosis Announces FDA Approval of IND for Use of ViXomeTM in COVID-19 ‘Post Covid Syndrome’

Oasis Psychiatric Day Program Achieves Prestigious Behavioral Health Care and Human Services Accreditation from The Joint Commission

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