Latest news on DFB and affiliated companies, NanOlogy and Phyton Biotech.
NanOlogy™ featured in PharmaVOICE article: Next-Generation Nanomedicines
(January 2018) — NanOlogy LLC managing director, Marc Iacobucci, was invited to contribute to a PharmaVOICE article on the future of nanotechnology in the pharmaceutical industry and how NanOlogy is using nanotechnology to transform the fight against cancer.
Phyton Biotech Unifies International Operations Under New Leadership
VANCOUVER, BC (December 21, 2017) —DFB announces the promotion of Colin Marr to President of Phyton Biotech, the world’s leader in commercial-scale plant cell fermentation technology and DFB’s wholly-owned subsidiary.
NanOlogy™ Announces First Patient Enrolled in a Pancreatic Cancer Phase 2 Clinical Trial of NanoPac® Adding to Trials in Prostate and Ovarian Cancers
DALLAS/FT.WORTH, (December 18, 2017) — NanOlogy LLC, a clinical-stage pharmaceutical development company, today announced the first patient has been enrolled in a clinical trial of NanoPac® (nanoparticle paclitaxel) sterile suspension administered intratumorally in patients with locally advanced pancreatic adenocarcinoma. The Phase 2a dose-rising trial will evaluate the safety and preliminary efficacy of NanoPac delivered directly into the tumor by endoscopic ultrasound-guided fine needle injection in patients who have completed current standard of care treatment prior to trial entry. NanoPac is part of an extensive submicron technology platform developed by NanOlogy. Gere diZerega, MD, VP of Medical Affairs, will present an overview of the platform and an update of the clinical program at Biotech Showcase™, on January 8, 2018 at 3:45PM in Franciscan room D (Ballroom Level) of the Hilton San Francisco Union Square.
Phyton Biotech Wins Grant from Bill & Melinda Gates Foundation to Develop New Approaches to Manufacturing Artemisinin Pancreas
AHRENSBURG, Germany, (November 29, 2017) — Phyton Biotech today announced that it has received a $400,000 grant from the Bill & Melinda Gates Foundation to fund the research and development of an alternative method of producing artemisinin, a key active pharmaceutical ingredient (API) used to combat malaria. Artemisinin-based therapies are the global standard for the treatment of malaria, a disease that affects over 200 million people annually and is on the rise. The API is derived from the leaves of the herb Artemisia annua or sweet wormwood, a plant that is primarily harvested in Asia for the critical drug ingredient. With demand expected to continue to grow over the next twenty years, alternative methods of commercially producing the vital drug ingredient will be needed to ensure adequate, sustainable supply and stable prices.
NanOlogy™ Announces First Patient Enrolled in a Phase 2 Clinical Trial of NanoPac® for Treatment of Mucinous Cysts of the Pancreas
DALLAS/FT.WORTH, (November 7, 2017) — NanOlogy LLC, a clinical-stage pharmaceutical development company, today announced the first patient has been enrolled in a clinical trial of NanoPac® (nanoparticle paclitaxel) sterile suspension for treatment of mucinous cystic neoplasms (MCNs) of the pancreas. The Phase 2 dose-rising trial will evaluate the safety and preliminary efficacy of NanoPac delivered directly into MCNs by endoscopic ultrasound-guided fine needle injection.
NanOlogy™ Announces First Patient Enrolled in a Phase 2 Clinical Trial of NanoPac® for Treatment of Prostate Cancer
DALLAS/FT.WORTH, (October 16, 2017) — NanOlogy LLC, a clinical-stage pharmaceutical development company, today announced the first patient has been enrolled in a clinical trial of NanoPac® (nanoparticle paclitaxel) sterile suspension administered into the prostate for treatment of prostate cancer. Part of a broad nanoparticle technology platform developed by the company, NanoPac will be evaluated for safety and preliminary efficacy in a dose-rising Phase 2(a) clinical trial following intratumoral injection of the prostate via transrectal ultrasound guidance in patients four weeks prior to radical prostatectomy.
NanOlogy™Announces First Patient Enrolled in a Phase 2 Clinical Trial of NanoPac® for Ovarian Cancer
DALLAS/FT.WORTH, (October 9, 2017) —NanOlogy LLC , a clinical-stage pharmaceutical development company, today announced enrollment of the first patient in a Phase 2 clinical trial of intraperitoneally (IP) administered NanoPac® (nanoparticle paclitaxel) sterile suspension in patients with ovarian cancer. Part of a broad nanoparticle technology platform developed by the company, NanoPac will be evaluated for safety and efficacy after IP instillation of NanoPac at the end of cytoreductive (debulking) surgery.
NanOlogy™ to present at Bio investor forum on October 17, 2017 in san Francisco
DALLAS/FT.WORTH, (September 26, 2017) —NanOlogy™, a clinical-stage pharmaceutical development company, announced today that VP of Medical Affairs Gere diZerega, MD, will present at the BIO Investor Forum conference Tuesday, October 17 at 9:45 am at the Westin St. Francis in San Francisco. The presentation will cover the status of the company’s clinical development program and how its nanoparticle technology platform aims to transform systemic chemotherapy into local delivery of proven drugs.
DFB Soria gives update on enrollment of phase 2 clinical trial of sor007 (nanoparticle paclitaxel) ointment for actinic keratosis (AK)
DALLAS/FT.WORTH, (September 26, 2017) —DFB Soria, a clinical-stage pharmaceutical development company, and an affiliate of NanOlogy™, today announced completion of the second of four patient cohorts enrolled in a Phase 2 actinic keratosis (AK) clinical trial of a topical ointment containing nanoparticle paclitaxel formed by a proprietary production process. Identified as SOR007, the ointment is being evaluated topically in a dose escalating trial for safety and preliminary efficacy.
drug development and delivery article on formation of NanOlogy & Soria for Clinical Development of Naked Nanoparticle Platform
September 14, 2017 – Demand for new cancer drugs is enormous with public and private investment skyrocketing for new technologies. Immunotherapies have captured much of the attention in recent years, but the first generation of these drugs has not delivered the hoped for panacea and development of more effective, safer immunotherapies is still years from reaching patients. In addition, immunotherapy is extremely expensive with treatment costs easily reaching $100,000 or more annually per patient.
DFB Pharmaceuticals Forms NanOlogy™ for Clinical Development of Naked Nanoparticle Platform to Treat Cancer and Related Illnesses
September 12, 2017 – DFB Pharmaceuticals, a private investment and development group, in collaboration with CritiTech and US Biotest, has formed NanOlogy to finance and develop a breakthrough technology platform to produce unique, patented, naked nanoparticle forms of paclitaxel and docetaxel for local delivery with the potential for greater efficacy and safety to treat cancer and other serious illnesses.
Texas Wesleyan and partners to honor Dorman at 48th Business Hall of Fame
July 7, 2017 – Texas Wesleyan University, the Fort Worth Business Press and the Fort Worth Chamber of Commerce are pleased to announce that Paul Dorman, CEO and chairman of DFB Pharmaceuticals, LLC, has been selected as the 2017 Fort Worth Business Executive of the Year.
Fort Worth entrepreneur, business executive provides tuition scholarships for new M.D. school
April 18, 2017 – In a show of support for the new TCU and UNTHSC School of Medicine, Fort Worth pharmaceutical executive, business investor and entrepreneur Paul Dorman will provide full first-year tuition to the inaugural class of medical students.
smith & nephew to acquire us bioactive wound care business for $782 million
November 28, 2012 – Smith & Nephew plc (LSE: SN, NYSE: SNN), the global medical technology business, today announces that it is strengthening its global position in advanced wound care by entering into an agreement through its subsidiaries to acquire substantially all the assets of Healthpoint Biotherapeutics (“Healthpoint”), a leader in bioactive debridement, dermal repair and regeneration wound care treatments, for $782 million in cash.
Roundtable healthcare partners portfolio company, renaissance acquisition holdings, LLC Acquires dpt Laboratories
LAKE FOREST, IL, July 5, 2012 — RoundTable Healthcare Partners (“RoundTable”), an operating‐oriented private equity firm focused exclusively on the healthcare industry, announced today that its portfolio company, Renaissance Acquisition Holdings, LLC (“Renaissance”), has acquired DPT Laboratories Inc. (“DPT”).