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Oct.11.2012

Regulatory Challenges for Cartilage Repair Technologies

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MCRA recently authored a peer-reviewed paper in the journal Cartilage entitled, “Regulatory Challenges for Cartilage Repair Technologies.” The complete article is in press and can be found at the journal’s website.

In the United States, few Food and Drug Administration (FDA)–approved options exist for the treatment of focal cartilage and osteochondral lesions. Developers of products for cartilage repair face many challenges to obtain marketing approval from the FDA.

In this journal article, we discuss the necessary steps for FDA application and approval for a new cartilage repair product, as cartilage repair therapies can receive market approval from FDA as medical devices, drugs, or biologics, and the specific classification of product can affect the nonclinical, clinical, and regulatory strategy to bring the product to market.

As discussed in the article, recent FDA guidance gives an outline of the required elements to bring a cartilage repair product to market, although these standards are often very general. As a result, companies have to carefully craft their study patient population, comparator group, and clinical endpoint to best showcase their product’s attributes. In addition, regulatory strategy and manufacturing process validation need to be considered early in the clinical study process to allow for timely product approval following the completion of clinical study.

Although the path to regulatory approval for a cartilage repair therapy is challenging and time-consuming, proper clinical trial planning and attention to the details can eventually save companies time and money by bringing a product to the market in the most expeditious process possible.

Sep.18.2012

Are You Ready (for UDI)?

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FDA has released the long-awaited proposed final rule for implementation of the unique device identification (UDI) regulation passed by Congress in 2007.  The initial 60-day comment period began on July 10, 2012.  FDA has extended the comment period until October 25, 2012.  Quoted from the Federal Register, Volume 77, Issue 180, “The Agency has received requests for a 45-day extension of the comment period for the information collection.  Each request conveyed concern that the current 60-day comment period does not allow sufficient time to develop a meaningful or thoughtful response to the information collection.”  The proposed rule can be found and comments provided to FDA here.

The proposed rule further states, “Under the proposed system, the health care community and the public would be able to identify a device through a UDI that will appear on the label and package of a device.  The UDI will provide a key to obtain critical information from a new database, the Global Unique Device Identification Database (GUDID), which will include information important to the identification of devices.”  UDI is based on automatic identification and data capture (AIDC) technology and will follow established international technical standards.  The standards are included in the proposed new 21 CFR Part 830, Unique Device Identification.

So what is UDI?  Simply stated, on the FDA website, “A UDI is a unique numeric or alphanumeric code that includes a device identifier, which is specific to a device model, and a production identifier, which includes the current production information for that specific device, such as the lot or batch number, the serial number and/or expiration date.”

And lastly, why this posting asks are you ready?  The proposed revision of 21 CFR Part 801 – Labeling, has the following information on the effectiveness of when UDI must be on devices after the publication date of the final rule:

  • Class III medical device or a device licensed under the Public Health Service Act – 1 Year
  • Class II – 3 Years
  • Class I and devices not classified – 5 Years

The bottom line – FDA has issued a proposed final rule and is expecting industry to be ready to comply with the regulation once it is final.

 

Sep.13.2012

Webinar Announcement: Case-by-Case Approval: Improving the Communication of Key Evidence to Secure Coverage

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MCRA’s Health Economics, Reimbursement & Public Policy division will be presenting an Elsevier Business Intelligence Webinar entitled “Case-by-Case Approval: Improving the Communication of Key Evidence to Secure Coverage” on September 27, 2012. Please click here for additional details and registration information for this upcoming webinar.

Webinar Summary: As health plans place more and more roadblocks for coverage of new technologies and procedures, the technology company’s strategy for handling denied cases becomes even more important. Most companies offer a billing guide or reimbursement toolkit to providers and other stakeholders, but often these resources lack specificity and key information that demonstrate the need for patient access to the technology or procedure.

During this webinar, Tim Hunter, Vice President of Health Economics, Reimbursement & Public Policy and Tina Murphy, Senior Manager, Patient Access Management, will provide an overview of current new technology denial trends, describe the importance of providing detailed prior authorization and claims denial resources to providers and patients, and offer recommendations to ensure that health plan decision makers are approving or denying a case based upon the correct evidence.

Please do not hesitate to get in touch with me at 202-552-5811 or by email at ebaldacchino@mcra.com if you have any questions regarding this webinar or MCRA’s reimbursement consulting services.

Aug.13.2012

FDA Regulation of Cellular Products Generated from a Patient’s Own Cells

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On August 7, 2012, the Wall Street Journal posted an opinion piece entitled, “The FDA Wants to Regulate Your Cells”. In this article, the authors cite a decision 2 weeks ago in US District Court where the FDA had sued Regenerative Sciences, LLC, to cease providing stem-cell based treatments due to lack of marketing approval. The US District Court agreed with the FDA in this litigation.

In the United States, human tissue products are generally exempt from pre-market review by the FDA, provided they meet certain requirements. One of these requirements is that the tissues be “minimally manipulated”. Examples of human tissue that meets the “minimally manipulated” standard include organ transplants, blood transplants, allograft bone processed to remove lipids and cells, bone demineralized via acid treatment, and production of autologous platelet rich plasma (PRP) using a centrifuge for bed-side treatment. As such, all of these treatments are exempt from FDA pre-market review, except the centrifuge that produces the PRP.

However, the process used by Regenerative Sciences is described as follows:

“This procedure, called the RegenexxTM procedure, is used to treat certain orthopedic conditions, such as osteoarthritis, nonhealing bone fractures, avascular necrosis and bulging lumbar discs. In this procedure, the physician takes bone marrow from the patient’s hip or synovial fluid from the patient’s knee, as well as blood from the patient, and transports these materials to a nearby laboratory facility.

At this facility, mesenchymal stem cells are isolated from the bone marrow or synovial fluid and expanded in culture for two to three weeks using growth factors from the patient’s blood, as well as other chemical reagents. The cells are then combined with drug products, such as doxycycline, which have been previously approved by the FDA, and are then transported back to the clinic for injection into the patient.”

The district court sided with the FDA in deciding that process Regenerative Sciences utilized for processing the cells fell beyond the scope of “minimal manipulation”.

However, FDA’s view that these processing methods fall beyond the scope of “minimal manipulation” is not new. Genzyme’s Carticel, FDA approved under a Biologics Licensing Application (BLA) since 1997, is a procedure similar to the one outlined by Regenerative Sciences. Carticel is produced by isolating a small portion of a patient’s knee cartilage, from which the patient’s cells are isolated, expanded in cell culture, and re-injected into the patient.

In particular, the expansion of cells, which involves the addition of many reagents and growth factors in a sterile environment, is the key step that takes the production process beyond minimal manipulation. Many chemical entities are added to stimulate the cells to divide and grow to obtain enough cells for therapeutic success. These processes, as demonstrated by laboratory science, can change the nature of the cells such that they are not necessarily the same as the ones removed from the patient. While these changes could be beneficial in some circumstances (such as increased ability to repair damaged tissues in the body), there is inherent risk that the cells could cause an adverse reaction in the patient due to these changes to the cells. In FDA’s view, these treatments should be held to the same standards of safety and effectiveness as drugs and medical devices prior to use.

The WSJ article authors state:

“Federal regulators have stretched that definition to the point where a reasonable limit no longer exists. The law provided a clear impediment to unrestrained exercise of FDA authority. Something needed to be an “article”—not a medical procedure—in order to become a drug. The constraint that a drug needed to be a “thing” has been read out of the law by FDA, and the district court appears to have accepted that position.

If human cells processed by the Colorado doctors are “drugs” under federal law, even when these cells are returned to the same patient who donated them, there may be little to prevent the FDA from imposing its drug-approval requirements on any cell-based procedure.”

The authors’ inferences that the FDA is ever-stretching its boundaries of its review and that they can impose requirements on any cell-based procedure are misleading. As demonstrated by the Carticel example, this view by the FDA of cultured cells as being medical products, even if sourced from a patient’s own cells, is a 15 year old precedent. Furthermore, regulations prevent the FDA from reviewing many types of cellular procedures involving a patient’s own cells, provided they meet the “minimal manipulation” standard. Regulatory precedent has demonstrated that procedures involving separation of cells via centrifugation, simple mixing of cells (as in in vitro fertilization), and implantation without culture of these cells clearly fall within the boundaries of minimal manipulation.

In its current view, the FDA requires rigorous non-clinical and clinical data to determine the safety and effectiveness of these cellular-based treatments.  While stem cell treatments and other cell-based treatments can provide exciting advances in the practice of medicine, the safety and effectiveness of these treatments have yet to be determined and successful results from isolated case reports should be viewed with scrutiny.

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