Paul J. Molino 

Paul Molino is one of the founding partners of Rakoczy Molino Mazzochi Siwik LLP. He is registered to practice before the United States Patent and Trademark Office and holds a Bachelor of Science in Pharmacy. Mr. Molino has extensive experience handling complex patent infringement litigation matters in federal courts throughout the United States, withparticular emphasis and expertise in the pharmaceutical and chemical industries. Mr. Molino serves as FDA regulatory counsel in a variety of high-stakes proceedings for national and international pharmaceutical, chemical and biotechnology companies.

Intellectual Property Litigation and Counseling-Hatch-Waxman, Patent,Trade Secret and Trademark

Mr. Molino has extensive experience handling and litigating highly specialized Hatch-Waxman statutory patent infringement and other actions on behalf of generic pharmaceutical companies involving prescription pharmaceutical drugs. Mr. Molino's experience extends from pre-litigation counseling up and through trial, and includes numerous trials through verdict just in the past few years, along with preliminary injunction proceedings. His litigation experience includes such blockbuster drugs as Neurontin® (gabapentin), Paxil® (paroxetine hydrochloride), Pravachol® (pravastatin sodium), Zoloft® (sertraline hydrochloride), Tricor® (fenofibrate), Antara® (fenofibrate), Ceftin® (cefuroxime axetil), Depakote® (divalproex sodium), Zantac® (ranitidine hydrochloride), Glucophage® (metformin hydrochloride), Omnicef® (cefdinir), Altace® (ramipril), Wellbutrin XL® (buproprion), Effexor XR (venlafaxine), Xopenex® levalbuterol, Keppra® (levetiractam), Megace® (megestrol acetate); Fosomax® (alendronate), Clarinex® (desloratadine), Trilepta® (oxcarbazepine), Femara® (letrozole), Lipitor® (atorvastatin), Crestor (rosuvastatin), Uroxatral® (alfuzosin), Cymbalta® (duloxetine), Namenda® (memantine), Pulimicort Respules® (budesonide), Carbetrol® (carbamazepine), Lunesta® (eszopiclone), Oracea® (doxycycline), Evoxac® (cevimeline) and others.

Mr. Molino's latest victory occurred on May 19, 2009, when the Federal Circuit issued a ruling affirming the U.S. District Court of the Eastern District of Virginia's finding that Lupin's generic Cefdinir drug does not infringe U.S. Patent No. 4,935,507. This victory allowed Lupin to continue marketing its Cefdinir product in the U.S. Moreover the case was a long awaited en banc opinion setting the new standard relating to "product by process" claims...finally resolving the split between the holding in Scripps and the holding in Atlantic Thermoplastics.

Mr. Molino also assisted in obtaining a final judgment of invalidity before the United States Court of Appeals for the Federal Circuit (Federal Circuit) on GlaxoSmithKline's main patent for Paxil®, one of the world's best selling antidepressants. Mr. Molino was a member of the trial team that won a decision of noninfringement on that patent in the district court before Judge Richard A. Posner. This trial victory received national attention and was highlighted in the American Lawyer, National Law Journal, New York Times and other national publications. More recently, Mr. Molino assisted in defeating a motion for a temporary restraining order and preliminary injunction relating to the prescription drug Altrace® (ramipril). This victory enabled the firm's client, Lupin, to immediately launch its product onto the U.S. Market.

Mr. Molino was involved in the Neurontin® (gabapentin) litigation, and assisted in obtaining two district court judgments of noninfringement for his pharmaceutical clients on two of Pfizer's patents for that multi-billion dollar prescription drug. He was also involved in the ground-breaking decision for generic drug industry on "off-label" method use of patents relating to gabapentin.

Mr. Molino's practice also includes counseling clients regarding patent strategies and developing and protecting intellectual property rights, including identifying and creating design-around opportunities and counseling on patent scope and validity issues.

Food and Drug and Hatch-Waxman Regulatory Litigation and Counseling

Mr. Molino counsels pharmaceutical and other companies in regulatory matters before the Food and Drug Administration (FDA), with particular expertise in Hatch-Waxman and related issues involving abbreviated new drug applications (ANDAs), section 505(b)(2) applications, and new drug applications (NDAs). He provides counseling on regulatory and compliance, approval, labeling and good manufacturing issues for ANDAs, 505(b)(2) applications and drug master files (DMFs). Mr. Molino has developed a detailed understanding of the scientific, business and legal issues important to pharmaceutical companies.

Previous Experience

Prior to founding Rakoczy Molino Mazzochi Siwik LLP, Mr. Molino was a partner in the national law firm of Lord, Bissell & Brook LLP. He joined that firm as an associate in 1994 and was elected to partnership in 2000.