Showing posts with label trialnet. Show all posts
Showing posts with label trialnet. Show all posts

Saturday, July 17, 2021

TrialNet In General

I have blogged dozens of times on clinical trials run by TrialNet, but I've never discussed TrialNet as an organization, so this blog contains some information on TrialNet, starting with their web site:
 
A Little History
 
The pre-history of TrialNet traces back to a large study called Diabetes Prevention Trial of Type 1 (DPT-1) which started 1994, which was testing oral insulin as a prevention of T1D.  TrialNet was formally founded in 2001, and (for me) is best known for their huge study now called "Pathway to Prevention" (previously called "Natural History Study").  This study is central to the mission of preventing T1D, by both (a) studying what is the normal progression of T1D and (b) creating a large pool of people in the process of developing T1D, which makes prevention focused clinical trials much easier to run. 

Kevan C. Herold of Yale University became chair of TrialNet on June 1st, 2021.  Prior to that, from 2015 to 2021, Carla J. Greenbaum of the Benaroya Research Institute was the chair, and before that, Jay Skyler.  Carla Greenbaum continues to direct the TrialNet Clinical Hub.
 
In writing this, I searched for a concise history of TrialNet, but was not able to find anything.  So if you have an interest in the history of science, this might make a great paper, or even a thesis.  Also, I was not able to find any public organizational or governance materials, so can't include any information on how TrialNet decisions are made.

Goals and Methods

TrialNet's goal is to prevent, delay and slow the progression of the T1D.  I would describe their basic method as a research funnel:
  1. They start out screening relatives of people with T1D, looking for those who have autoimmune antibodies.
  2. They then follow those people to see if the number of autoimmune antibodies increases, if they start having higher than normal blood glucose after eating carbohydrates, and if they are diagnosed with T1D.
  3. For those who develop T1D, they follow them to see how the disease evolves over time.

Throughout this whole process, they are recruiting people for more specific studies to test preventions or cures appropriate to their stage in the disease. 

Without TrialNet, if a researcher wanted to recruit 50 people at-risk for type-1 diabetes from the general population, they would need to test thousands of people to find the 50 they were looking for.  That process alone would likely take years and cost hundreds of thousands, if not millions, of dollars.  Even if they could focus on the relatives of people with T1D, they would still need to test 100s of people, and it would still cost a lot and take a long time.  But TrialNet has already found many people who can participate in those studies.

Research Achievements

I consider the following items to be TrialNet's three biggest achievements in chronological order: 
 
First: showing the normal progression of T1D.  In particular documenting the length of the honeymoon period, and what should be expected during that time.  To understand why this is important, consider the saga of BCG.  In the 1990s there was a small clinical trial which gave BCG to six people with newly diagnosed type-1 diabetes (no control group).  One of them went a few weeks without injecting insulin.  At the time (before the TrialNet results), this triggered a lot of optimism, including at least three follow-on studies.  The follow-on studies all had control groups and all failed, because (in fact) that result is pretty normal for the honeymoon period without any treatment at all.  With the TrialNet information, researchers do not waste their time following up these "normal, but we didn't know it was normal" results.  Also, there is now much more and much better information on what should be expected during the honeymoon period, which is a very stressful time for everyone involved.
 
Second, showing that a person who tests positive for two autoantibodies would later develop T1D in nearly all cases.   This process might take up to 10 years, but it would eventually happen.  Without TrialNet we would not know how number of autoantibodies related to chance of being diagnosed with T1D, or how long it would take on average.  The whole idea of using number of autoantibodies to predict chances of being diagnosed with T1D is based on TrialNet data.

I know that many people are unhappy with this knowledge, especially when their kids test positive for those first two autoantibodies.  However, this knowledge has opened up a wide range of research to try and prevent this diagnoses which would never have been possible without it.

Third,  Teplizumab, which I've blogged on before:
TrialNet did the earliest research into Teplizumab, and they continued researching Teplizumab even when clinical trials run by commercial companies were unsuccessful.  This dogged determination led directly to Teplizumab's current status. In November 2020, Teplizumab was submitted for marketing approval by the FDA for preventing or delaying the onset of T1D when given to people at-risk of the disease.  (Obviously, I'll blog if it is approved.)  If approved it will be a huge breakthrough: the first treatment to delay the onset of T1D.  More than that, the first treatment to change the immune reaction which causes T1D.  First treatments are rarely perfect, but even if not perfect, they often point the way to better treatments, and TrialNet was key to Teplizumab's research success.

Current Research

List of TrialNet's honeymoon research:
    http://www.trialnet.org/our-research/newly-diagnosed-t1d
List of TrialNet's at-risk research:  

In addition to TOPPLE T1D, which is for adults within 4 years of clinical diagnosis, TrialNet is
also running trials on Abatacept and Hydroxychloroquine (HCQ) for at-risk individuals.  In the past, TrialNet and has run multiple trials in honeymooners, most recently on ATG/GCSF, and also run two and oral insulin trials in people at risk of T1D.

By far the largest research project is TrialNet’s Pathway to Prevention which is focused on Risk Screening and Monitoring.  These are cooperative large scale monitoring trials, involving tens of thousands of people.  Relatives of people with T1D are tested for autoantibodies, and then monitored or enrolled in prevention trials if autoantibodies are found.  If they develop T1D, its progression is followed through the LIFT study. TrialNet's prevention studies are open to anyone who has  autoantibodies, no matter if they have relatives with T1D or not.

In the past, I know that some people did not want to participate in risk screening style research, because they "didn't want to know if there was nothing they could do".  However, that thinking is now out of date.  Because of several clinical studies underway to prevent or delay T1D, there now is something you can do, if you know ahead of time.  Furthermore, if Teplizumab is approved, then there will be a treatment available to delay the onset of T1D.

Also, these risk screening projects have been critical to learning how T1D naturally progresses, and also to finding people to participate in the more specific prevention and delay studies mentioned above.  So participants are helping to move forward important parts of T1D research, no matter how much they personally benefit during the study.

A final word about terminology: TrialNet uses a four stage timeline of T1D progression described here:
The basic summary is that stages 1 and 2 are people who have two or more autoantibodies [definition], but no symptoms that a patient would notice.  Stage 3 is honeymoon, and stage 4 is established type-1 diabetes.  However, this is not the terminology used (or understood) by most people effected by T1D, which is why I use more informal terminology: "at-risk" meaning people with 2 or more antibodies, but no symptoms (stage 1 and 2 in TrialNet terminology), and then "honeymoon" for stage 3 and "established" for stage 4.

More Reading


Joshua Levy
http://cureresearch4type1diabetes.blogspot.com
publicjoshualevy at gmail dot com
All the views expressed here are those of Joshua Levy, and nothing here is official JDRF or JDCA news, views, policies or opinions. My daughter has type-1 diabetes and participates in clinical trials, which might be discussed here. My blog contains a more complete non-conflict of interest statement. Thanks to everyone who helps with the blog.

Sunday, April 4, 2021

Novo Nordisk and TrialNet Start TOPPLE T1D: Phase-I Trial of Four Protein Plasmid

This clinical trial is testing NNC0361-0041 which is a four protein plasmid. The drug was developed by Novo Nordisk, and the trial is being run by TrialNet. A plasmid is a bit of DNA which is not attached to the cell's main DNA.  You can think of it as a delivery service to get other molecules into a cell.  The other molecules, in this case, are four proteins: pre-proinsulin, TGF-β1, IL-10 and IL-2.  Pre-proinsulin is a chemical that is made by cells as part of the process to create insulin.  Pre-proinsulin is converted to proinsulin, which is converted to insulin.  The other three are proteins used by the immune system to communicate.  All of them have been subjects of clinical trials in the hopes they would cure/treat T1D.  So there is some appeal in the idea of using them all at once, and the plasmid is a convenient way to get all of them into cells together. 

I'm working on a blog posting which describes TrialNet, and which should come out in a month or so.

This Study

This study has a lot crammed into it.  It is the first test in people, so a phase-I trial.  However, it will enroll a total of 48 people, so closer in size to most phase-II trials.  The people will be grouped into four cohorts.  Each cohort will get a larger dose than the previous cohort, and each will have its own control group (9 treated and 3 controls per cohort).  Each cohort will be followed for a year.  The study started in Nov 2020 and they plan to finish in July 2022.

This study is open to adults (18 to 45 years old) within 4 years of T1D diagnosis; it is not limited to people in the honeymoon phase.

The primary outcome of this study is adverse events, so it is focused on safety.  However, the secondary outcome measures C-peptide, which measures how much insulin is being generated and measures progress to a cure.  The treatment will be weekly subcutaneous injections for 12 weeks.  (Subcutaneous injections are the same type as used for insulin.)

Recruiting
 
This study is recruiting all over the United States.  The entire list of recruiting sites is listed at the end of the blog.  For recruitment and enrollment related questions contact: info@trialnet.org
 
If you are a relative of someone with T1D, and want to learn about TrialNet's "Pathways to Prevention" trial, there is information here: https://trialnet.org/participate

Discussion

What really jumped out at me, was how much information they are going to get from one fairly quick study.  Normally, a phase-I trial is small.  It tests on a small number of people with a small dose.  But this study combines many of the goals of a phase-I and phase-II trial into one (especially in terms of testing multiple doses and on a total of almost 50 people).  I also like the speed of this study: less than 2 years from start of recruitment to expected results.  I just hope they are successful in recruiting enough people quickly enough to make that timeline.

While TrialNet has in the past partnered with industry to assure access to drugs, to the best of my knowledge, this is the first time TrialNet and a commercial drug company have worked together on a clinical study like this.  I think that this is an important step forward for T1D research in general. TrialNet is in a unique position to recruit people who are at-risk of T1D, but have not yet shown symptoms.  Commercial companies are well suited to develop treatments which might prevent or delay the onset of T1D.  So having these two working together plays to each of their strengths.   


Wikipedia pages:  

Trial Web Page:  https://www.trialnet.org/our-research/newly-diagnosed-t1d/TOPPLE
Clinical Trial Record:  Clinical Trial Record for NCT04279613

A personal note on the small size of the world:  In the 1970s, when I was a kid, I was called "little Josh".  That was because my family was friends with another family whose father was Joshua Lederburg, who we called "big Josh".  At the time, as a 10 year old, I knew that Big Josh was a smart guy who worked at Stanford University.  As it turns out, Joshua Lederburg was the scientist who named the plasmid in a paper he wrote in 1952. Six years later, he would be awarded the Nobel prize for related research.  In a sense, the clinical trial I'm reporting here is the 70 year follow on to the breakthrough he made back then.
 
List of Recruiting Sites

Stanford University
Stanford, California, United States, 94305
Contact: Trudy Esrey    650-498-4450    tesrey@stanford.edu        

Barbara Davis Center at University of Colorado Anschutz Medical Campus 
Aurora, Colorado, United States, 80045
Contact: Morgan Sooy    303-724-5686    MORGAN.QUIST@CUANSCHUTZ.EDU         

Yale University School of Medicine 
New Haven, Connecticut, United States, 06519
Contact: Laurie Feldman    203-737-2760    laurie.feldman@yale.edu        

University of Florida 
Gainesville, Florida, United States, 32610
Contact: Jennifer Hosford    352-294-5759    jennifer.hosford@peds.ufl.edu        

Indiana University - Riley Hospital for Children
Indianapolis, Indiana, United States, 46202
Contact: Maria Spall    317-278-8879    malnicho@iu.edu         

Joslin Diabetes Center
Boston, Massachusetts, United States, 02215
Contact: Nora Bryant    617-309-4141    nora.bryant@joslin.harvard.edu        

University of Minnesota
Minneapolis, Minnesota, United States, 55466
Contact: Janice Leschyshyn    612-626-8467    lesch004@umn.edu       

The Children's Mercy Hospital 
Kansas City, Missouri, United States, 64108
Contact: Jennifer James    913-696-5059    jljames@cmh.edu        

The Naomi Berrie Diabetes Center at Columbia University Medical Center
New York, New York, United States, 10032
Contact: Sarah Pollak    212-851-5425    sjp2174@columbia.edu     

University of Pittsburgh
Pittsburgh, Pennsylvania, United States, 15224
Contact: Kelli DeLallo    412-692-5210    kelli.delallo@chp.edu  
    
Benaroya Research Institute
Seattle, Washington, United States, 98101
Contact: Corinna Tordillos    206-341-8937    ctordillos@benaroyaresearch.org
 
UCSF
San Francisco, California
Contact: Karen Ko 
415-514-3730  karen.ko@ucsf.edu

University of Texas Southwestern
Dallas, Texas
Contact: Lindsay Harter
214-648-4725 Lindsay.Harter@UTSouthwestern.edu

Emory University
Atlanta, Georgia
Contact: Xiaomiao Lan-Pidhainy 
404-712-0051 xlanpid@emory.edu

Vanderbilt University
Nashville, Tennessee
Contact: Brenna Hammel
(615) 337-9597 brenna.hammel@vumc.org

Children’s Hospital of Orange County
Orange, California
Contact: Heather Speer
(714) 509-8613 hspeer@choc.org
 




Joshua Levy
http://cureresearch4type1diabetes.blogspot.com
publicjoshualevy at gmail dot com
All the views expressed here are those of Joshua Levy, and nothing here is official JDRF or JDCA news, views, policies or opinions. My daughter has type-1 diabetes and participates in clinical trials, which might be discussed here. My blog contains a more complete non-conflict of interest statement. Thanks to everyone who helps with the blog.