One or More Clinical Trials to get FDA Approve a Drug?
Reporter: Aviva Lev-Ari, PhD, RN
Almost half of all new drug approvals in 2018 relied on one clinical trial

SOURCE
Posted in FDA, FDA Regulatory Affairs on May 15, 2019| Leave a Comment »
Reporter: Aviva Lev-Ari, PhD, RN

SOURCE
Posted in Cancer - General, Cancer and Current Therapeutics, CANCER BIOLOGY & Innovations in Cancer Therapy, Cancer Informatics, Cancer Screening, CT, FDA, FDA Regulatory Affairs, FDA, CE Mark & Global Regulatory Affairs: process management and strategic planning - GCP, GLP, ISO 14155, Fiction and medicine, Medical Imaging Technology, Medical Imaging Technology, Image Processing/Computing, MRI, CT, Nuclear Medicine, Ultra Sound, Uncategorized on April 7, 2019| Leave a Comment »

3.5.2.6 Imaging: seeing or imagining? (Part 2), Volume 2 (Volume Two: Latest in Genomics Methodologies for Therapeutics: Gene Editing, NGS and BioInformatics, Simulations and the Genome Ontology), Part 3: AI in Medicine
That is the question…
Anyone who follows healthcare news, as I do , cannot help being impressed with the number of scientific and non-scientific items that mention the applicability of Magnetic Resonance Imaging (‘MRI’) to medical procedures.
A very important aspect that is worthwhile noting is that the promise MRI bears to improve patients’ screening – pre-clinical diagnosis, better treatment choice, treatment guidance and outcome follow-up – is based on new techniques that enables MRI-based tissue characterisation.
Magnetic resonance imaging (MRI) is an imaging device that relies on the well-known physical phenomena named “Nuclear Magnetic Resonance”. It so happens that, due to its short relaxation time, the 1H isotope (spin ½ nucleus) has a very distinctive response to changes in the surrounding magnetic field. This serves MRI imaging of the human body well as, basically, we are 90% water. The MRI device makes use of strong magnetic fields changing at radio frequency to produce cross-sectional images of organs and internal structures in the body. Because the signal detected by an MRI machine varies depending on the water content and local magnetic properties of a particular area of the body, different tissues or substances can be distinguished from one another in the scan’s resulting image.
The main advantages of MRI in comparison to X-ray-based devices such as CT scanners and mammography systems are that the energy it uses is non-ionizing and it can differentiate soft tissues very well based on differences in their water content.
In the last decade, the basic imaging capabilities of MRI have been augmented for the purpose of cancer patient management, by using magnetically active materials (called contrast agents) and adding functional measurements such as tissue temperature to show internal structures or abnormalities more clearly.
In order to increase the specificity and sensitivity of MRI imaging in cancer detection, various imaging strategies have been developed. The most discussed in MRI related literature are:
T2 MRI pelvis with Endo Rectal Coil ( DATA of Dr. Lance Mynders, MAYO Clinic)
Axial MRI Lava DCE with Endo Rectal ( DATA of Dr. Lance Mynders, MAYO Clinic)
DW image of the left parietal glioblastoma multiforme (WHO grade IV) in a 59-year-old woman, Al-Okaili R N et al. Radiographics 2006;26:S173-S189
Source AJR: http://www.ajronline.org/content/196/6/W715/F3
In the last couple of years, medical opinion leaders are offering to use MRI to solve almost every weakness of the cancer patients’ pathway. Such proposals are not always supported by any evidence of feasibility. For example, a couple of weeks ago, the British Medical Journal published a study [1] concluding that women carrying a mutation in the BRCA1 or BRCA2 genes who have undergone a mammogram or chest x-ray before the age of 30 are more likely to develop breast cancer than those who carry the gene mutation but who have not been exposed to mammography. What is published over the internet and media to patients and lay medical practitioners is: “The results of this study support the use of non-ionising radiation imaging techniques (such as magnetic resonance imaging) as the main tool for surveillance in young women with BRCA1/2 mutations.”.
Why is ultrasound not mentioned as a potential “non-ionising radiation imaging technique”?
Another illustration is the following advert:
An MRI scan takes between 30 to 45 minutes to perform (not including the time of waiting for the interpretation by the radiologist). It requires the support of around 4 well-trained team members. It costs between $400 and $3500 (depending on the scan).
The important question, therefore, is: Are there, in the USA, enough MRI systems to meet the demand of 40 million scans a year addressing women with radiographically dense breasts? Toda there are approximately 10,000 MRI systems in the USA. Only a small percentage (~2%) of the examinations are related to breast cancer. A
A rough calculation reveals that around 10000 additional MRI centers would need to be financed and operated to meet that demand alone.
References
http://radiographics.rsna.org/content/26/suppl_1/S173.full
Posted in BioSimilars, Drug Development Process, FDA, FDA Regulatory Affairs, FDA, CE Mark & Global Regulatory Affairs: process management and strategic planning - GCP, GLP, ISO 14155, Patient Experience: Personal Memories of Invasive Medical Intervantion, Value-based Drug Pricing, tagged Biopharmaceutical, FDA, FDA commisioner, Food and Drug Administration, health costs, New Drug Application, Personalized and Precision Medicine & Genomic Research, pharma, Pharmaceutical industry, Scott Gottlieb on March 8, 2019| Leave a Comment »
Reporter: Stephen J. Williams, Ph.D.

Also under his command, the FDA took quick and decisive action on drug costs. The commissioner worked to boost generic approvals and crack down on regulatory “gaming” that stifles competition. He additionally blamed branded drug companies for an “anemic” U.S. biosimilars market and recently blasted insulin pricing.
His sudden departure will likely leave many agency efforts to lower costs up in the air. After the news broke, many pharma watchers posted on Twitter that Gottlieb’s resignation is a loss for the industry.
During his tenure as FDA commissioner, Gottlieb’s name had been floated for HHS chief when former HHS secretary Tom Price resigned due to a travel scandal, but Gottlieb said he was best suited for the FDA commissioner job. Now, former Eli Lilly executive Alex Azar serves as HHS secretary, and on Tuesday afternoon, Azar praised Gottlieb for his work at the agency.
Also read from FiercePharma:
AUDIT Podcast


WASHINGTON — Dr. Norman E. (Ned) Sharpless, director of the National Cancer Institute, will serve as acting commissioner of the Food and Drug Administration, Alex M. Azar III, secretary of health and human services, announced on Tuesday.
Dr. Sharpless temporarily will fill the post being vacated by Dr. Scott Gottlieb, who stunned public health experts, lawmakers and consumer groups last week when he abruptly announced that he was resigningfor personal reasons.
Dr. Sharpless has been director of the cancer center, part of the National Institutes of Health, since October 2017. He is also chief of the aging biology and cancer section in the National Institute on Aging’s Laboratory of Genetics and Genomics. His research focuses on the relationship between aging and cancer, and development of new treatments for melanoma, lung cancer and breast cancer.
“Dr. Sharpless’s deep scientific background and expertise will make him a strong leader for F.D.A.,” said Mr. Azar, in a statement. “There will be no let up in the agency’s focus, from ongoing efforts on drug approvals and combating the opioid crisis to modernizing food safety and addressing the rapid rise in youth use of e-cigarettes.”
Dr. Douglas Lowy, known for seminal research on the link between human papillomavirus and multiple cancer types including cervical, and ultimately leading to development of a vaccine, will be named head of the NCI to replace Dr. Sharpless. Dr. Lowy currently is Deputy Director of the NCI.
Regulatory Affairs: Publications on FDA-related Issues – Aviva Lev-Ari, PhD, RN
FDA Approves La Jolla’s Angiotensin 2
FDA Approval marks first presentation of bivalirudin in frozen, premixed, ready-to-use formulation
Skin Regeneration Therapy One of First Tissue Engineering Products Evaluated by FDA
‘Landmark FDA approval bolsters personalized medicine’ by Edward Abrahams, PhD, President, PMC
Posted in Chronic Thromboembolic Pulmonary Hypertension (CTEPH) and Pulmonary Arterial Hypertension (PAH), Drug Carrier Design, Drug Delivery Platform Technology, FDA, FDA Regulatory Affairs, tagged angiotensin 2, ATHOS-3 trial, Critical Care, FDA approval on March 5, 2019| Leave a Comment »
Reporter: Irina Robu, PhD
In La Jolla Pharmaceutical Company’s new drug application (NDA) for angiotensin 2, the treatment was given priority review status by the FDA, advancing the application process to 6 months. The US Food and Drug Administration has approved an IV agent to treat critically-low blood pressure angiotensin 2 injection (Giapreza) for the treatment of adults with septic or other distributive shock. The intravenous infusion therapy is considered to increase blood pressure in adult patients with hypotension. The condition can cause shock in which the brain, kidneys, and other vital organs are no longer getting the appropriate amount of blood flow to function correctly.
The trial was based on the 321-patient ATHOS-3 trial, in which 69.9% of patients with catecholamine-resistant hypotension treated with angiotensin II upgrading at hour 3 versus 23.4% with placebo. The exploratory therapy was run in combination with conventional treatments used to raise patients’ blood pressure. The treatment was revealed an increase blood pressure, reported safety and tolerability.
Even though the label indicates that the drug can cause thrombosis, concurrent prophylactic treatment should be used. In ATHOS-3, the incidence of arterial and venous thrombotic events was 13%, compared with 5% in the placebo group, mainly driven by deep vein thrombosis.
John A. Kellum, Director of Center for Critical Care Nephrology, University of Pittsburgh, said the treatment is now an additional tool for the critical care community.
SOURCE
Posted in Drug Development Process, FDA, CE Mark & Global Regulatory Affairs: process management and strategic planning - GCP, GLP, ISO 14155, Pharmaceutical Analytics, Pharmaceutical Drug Discovery, Pharmaceutical Industry Competitive Intelligence, Pharmaceutical R&D Investment on January 16, 2019| Leave a Comment »
Reporter: Aviva Lev-Ari, PhD, RN
BIOBUSINESS BRIEFS
Fig. 1 | FDA approvals of new therapeutic drugs and aggregate projected peak global annual sales: 2000–2018. We analysed 2018 FDA approvals of new therapeutic drugs (NTDs), defined as new molecular entities approved by the FDA’s Center for Drug Evaluation and Research (CDER) and Center for Biologics Evaluation and Research (CBER), but with two adjustments: first, we excluded diagnostic imaging agents; and second, we included combination products with at least one new molecular entity as an active ingredient. The analysis is based exclusively on approvals by the FDA and the year in which the first indication approval took place. All peak sales values were obtained from EvaluatePharma and were inflation-adjusted to 2018 using standard global GDP-based inflators sourced from the Economist Intelligence Unit. To arrive at peak sales for each NTD, we reviewed both historical actual sales as well as the full range of forecast sales that are available from EvaluatePharma and selected the highest value. Sources: EvaluatePharma, FDA and Boston Consulting Group analysis.
SOURCE
Posted in FDA Regulatory Affairs, Heart Failure (HF), Personalized and Precision Medicine & Genomic Research, Regenerative Biology and Medicine, Stem Cells for Regenerative Medicine on October 31, 2018| Leave a Comment »
Reporter: Aviva Lev-Ari, PhD, RN
https://www.thecrimson.com/article/2018/10/31/medical-school-paper-retracted/
NHLBI NEWS
Statement
Posted in FDA, FDA Regulatory Affairs, FDA, CE Mark & Global Regulatory Affairs: process management and strategic planning - GCP, GLP, ISO 14155, tagged polyneuropathy of hereditary transthyretin-mediated amyloidosis on October 18, 2018| Leave a Comment »
Reporter: Aviva Lev-Ari, PhD, RN
by Harvard-MIT Center for Regulatory Science
Free
Innovators in Therapeutics, a Student Speaker Series
Thu, November 15, 2018, 4:30 PM – 6:30 PM EST
Free
REGISTER
Please join us for the Innovators in Therapeutics student speaker series organized by the Harvard-MIT Center for Regulatory Science and the Harvard Program in Therapeutic Science. The first installment of this series will feature John Maraganore, the CEO of Alnylam, and Sara Nochur, Alnylam’s Senior Vice President for Regulatory Affairs. Dr. Maraganore and Dr. Nochur will describe Alnylam’s path through development and FDA approval of the first RNAi therapeutic, ONPATTRO™ (patisiran), for the treatment of polyneuropathy of hereditary transthyretin-mediated amyloidosis. Dr. Maraganore and Dr. Nochur will focus on the regulatory science aspects of gaining approval for this innovative therapeutic.
Prior to the seminar, please join us for a networking session that brings together faculty, students and trainees who are interested in translational research, pharmacology, biotechnology, and regulatory science. Following the speaking program, there will be a small group discussion for students and trainees to engage directly with the expert about the topic at hand. Participation in the small group discussion is limited to students who register and are confirmed prior to the event.
This event is free and open to the Boston research community. Please help us to plan by RSVPing here!
AGENDA
4:30 – 5:00pm: Pre-event reception (outside Cannon Room)
5:00 – 5:45pm: Innovators in Therapeutics with Alnylam’s John Maraganore & Sara Nochur (Cannon Room)
5:45 – 6:15pm: [Limited Space] Student and Trainee Q&A with John Maraganore & Sara Nochur (Folin Wu Room)
SOURCE
https://www.eventbrite.com/e/innovators-in-therapeutics-a-student-speaker-series-tickets-50806305026
Posted in BioTechnology - Venture Creation, BioTechnology - Venture Creation, Venture Capital, CANCER BIOLOGY & Innovations in Cancer Therapy, FDA Regulatory Affairs, Foundations for supporting Science and Education, Global Partnering & Biotech Investment, Intellectual Property, Innovations, Commercialization, Investment in technological breakthrough, Uncategorized, Venture Capital, tagged biotech startup, Biotechnology, early ventures, national cancer institute, National Institutes of Health (NIH) ’s Common Fund, NCI, SBIR, startup on September 27, 2018| Leave a Comment »
NIH SBIR Funding Early Ventures: September 26, 2018 sponsored by Pennovation
Stephen J. Williams PhD, Reporter
Penn Center for Innovation (Pennovation) sponsored a “Meet with NCI SBIR” program directors at University of Pennsylvania Medicine Smilow Center for Translational Research with a presentation on advice on preparing a successful SBIR/STTR application to the NCI as well as discussion of NCI SBIR current funding opportunities. Time was allotted in the afternoon for one-on-one discussions with NCI SBIR program directors.
To find similar presentations and one-on-one discussions with NCI/SBIR program directors in an area nearest to you please go to their page at:
https://sbir.cancer.gov/newsevents/events
For more complete information on the NCI SBIR and STTR programs please go to their web page at: https://sbir.cancer.gov/about
Budget levels were discussed as well as the waiver program, which allows for additional funds to be requested based on criteria set by NCI (usually for work that is deemed high priority or of a specialized nature which could not be covered sufficiently under the standard funding limits) as below:
Phase I: 150K standard but you can get waivers for certain work up to 300K
Phase II: 1M with waiver up to 2M
Phase IIB waiver up to 4M
You don’t need to apply for the waiver but grant offices may suggest citing a statement requesting a waiver as review panels will ask for this information
Fast Track was not discussed in the presentation but for more information of the Fast Track program please visit the website
NCI is working hard to cut review times to 7 months between initial review to funding however at beginning of the year they set pay lines and hope to fund 50% of the well scored grants
NCI SBIR is a Centralized system with center director and then program director with specific areas of expertise: Reach out to them
IMAT Program and Low-Resource Setting new programs more suitable for initial studies and also can have non US entities
Phase IIB Bridge funding to cross “valley of death” providing up to 4M for 2-3 years: most were for drug/biological but good amount for device and diagnostics
Also they have announced administrative supplements for promoting diversity within a project: can add to the budget
3 on biotherapies
2 imaging related
2 on health IT
4 on radiation therapy related: NOTE They spent alot of time discussing the contracts centered on radiation therapy and seems to be an area of emphasis of the NCI SBIR program this year
4 other varied topics
>70% of NCI SBIR budget went to grants (for instance Omnibus grants); about 20-30% for contracts; 16% for phase I and 34 % for phase II ;
ALSO the success rate considerably higher for companies that talk to the program director BEFORE applying than not talking to them; also contracts more successful than Omnibus applications
From the NCI SBIR website:
The Niche Assessment Program is designed to help small businesses “jump start” their commercialization efforts. All active HHS (NIH, CDC, FDA) SBIR/STTR Phase I awardees and Phase I Fast-Track awardees (by grant or contract) are eligible to apply. Registration is on a first-come, first-serve basis!
The Niche Assessment Program provides market insight and data that can be used to help small businesses strategically position their technology in the marketplace. The results of this program can help small businesses develop their commercialization plans for their Phase II application, and be exposed to potential partners. Services are provided by Foresight Science & Technology of Providence, RI.
Technology Niche Analyses® (TNA®) are provided by Foresight, for one hundred and seventy-five (175), HHS SBIR/STTR Phase I awardees. These analyses assess potential applications for a technology and then for one viable application, it provides an assessment of the:
Commercialization Acceleration Program (CAP)
From the NIH SBIR website:
NIH CAP is a 9-month program that is well-regarded for its combination of deep domain expertise and access to industry connections, which have resulted in measurable gains and accomplishments by participating companies. Offered since 2004 to address the commercialization objectives of companies across the spectrum of experience and stage, 1000+ companies have participated in the CAP. It is open only to HHS/NIH SBIR/STTR Phase II awardees, and 80 slots are available each year. The program enables participants to establish market and customer relevance, build commercial relationships, and focus on revenue opportunities available to them.
The I-Corps program provides funding, mentoring, and networking opportunities to help commercialize your promising biomedical technology. During this 8-week, hands-on program, you’ll learn how to focus your business plan and get the tools to bring your treatment to the patients who need it most.
Program benefits include:
ICORPS is an Entrepreneurial Program (8 week course) to go out talk to customers, get assistance with business models, useful resource which can guide the new company where they should focus on for the commercialization aspect
THE NCI Applicant Assistance Program (AAP)
The SBIR/STTR Applicant Assistance Program (AAP) is aimed at helping eligible small R&D businesses and individuals successfully apply for Phase I SBIR/STTR funding from the National Cancer Institute (NCI), National Institute for Neurological Disorders and Stroke (NINDS), National Heart, Lung and Blood Institute (NHLBI). Participation in the AAP will be funded by the NCI, NINDS, and NHLBI with NO COST TO PARTICIPANTS. The program will include the following services:
For more details about the program, please refer to NIH Notice NOT-CA-18-072.
These programs are free for first time grant applicants and must not have been awarded previous SBIR
Peer Learning Webinar Series goal to improve peer learning .Also they are starting to provide Regulatory Assistance (see below)
NIH also provides Mentoring programs for CEOS and C level
10. before you submit solicit independent readers
NCI SBIR can be found on Twitter @NCIsbir
I was able to sit down with Dr. Monique Pond, AAAS Science & Technology Policy Fellow, Health Scientist within the NCI SBIR Development Center to discuss the new assistance program in regulatory affairs she is developing for the NCI SBIR program. Dr Pond had received her PhD in chemistry from the Pennsylvania State University, completed a postdoctoral fellow at NIST and then spent many years as a regulatory writer and consultant in the private sector. She applied through the AAAS for this fellowship and will bring her experience and expertise in regulatory affairs from the private sector to the SBIR program. Dr. Pond discussed the difficulties that new ventures have in formulating regulatory procedures for their companies, the difficulties in getting face time with FDA regulators and helping young companies start thinking about regulatory issues such as pharmacovigilence, oversight, compliance, and navigating the complex regulatory landscape.
In addition Dr. Pond discussed the AAAS fellowship program and alternative career paths for PhD scientists.
A formal interview will follow on this same post.