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Status unknownNCT02112097ASISinPPUpdated Jun 24, 2015

ASIS for Enbrel in Plaque Psoriasis

A Phase 1/2 interventional study of Gadolinium and Gadolinium in Plaque Psoriasis., sponsored by ASIS Corporation. Status unknown at 2 sites in United States. Open to participants aged 21 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2015-06-24.

Sponsored by ASIS Corporation · Phase 1/2, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Jun 2015), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Phase 1/2
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
21 Years to 65 Years
Sex
All
01

Study summary

AUTOMATIC SUBDERMAL INJECTOR SYSTEM (ASIS) Corporation has developed and patented the only automatic injection system for delivery of injectable products to the optimum spot, just outside of the fascia, which exists subdermally (between the skin and muscle) or interfascial (between the deeper muscles). ASIS device creates that bloodless space, enhancing Enbrel's efficacy and preventing unnecessary distant spread and adverse reactions. This space remains bloodless as long as the skin is lifted up or filled with an injectable product. Although ASIS device was initially designed to best administer BOTOX for such muscular conditions as Upper limb Spasticity, Cervical Dystonia, Chronic Migraine, Strabismus, Blepharospasm, and Primary Axillary Hyperhidrosis, the technology will also benefit other injectable products, including: GAMMAGARD for Primary Immunodeficiency (PI) and Insulin for Diabetics, etc.

Read the detailed description

Over 6 months, Aim 1 will demonstrate that ASIS device consistently delivers an injectable product (e.g. Gadolinium) into that subdermal bloodless space. MRI is the most simple and logical imaging choice, preferred because with ultrasound, air is injected, which will dissipate too quickly out of bloodless space to allow measurements. Since there isn't a way to measure the level of Gadolinium within that subdermal bloodless space, at least the Prolongation of Gadolinium may be approximated by its greater or longer Persistent % on MRI. Also, since we can't assume that bloodless space for patients with a particular disease will behave the same way as normal patients or patients with different diseases, this approximation only works if the variables are minimized to the same particular skin affected by Plaque Psoriasis. Case in point, patients with Plaque Psoriasis tend to have thicker skin, so expectantly will have prolonged Gadolinium subcutaneously Persistent %, which may be very different from the other diseases and certainly from the skin of normal patients, while the Gadolinium subdermally Persistent % should remain the same. Therefore, the Relative Prolongation Ability Score or total Persistent % subdermally over total Persistent % subcutaneously, will be different and very specific for the particular skin affected by Plaque Psoriasis. However, they are valuable indicators that will help us modify the Enbrel dosage and duration to inject into that "unknown" subdermal space for Aim 2, from the "known" typical Enbrel dosage and duration for Plaque Psoriasis patients. For example, if Aim 1 found the Relative Prolongation Ability Score for the Plaque Psoriasis skin to be (2.00), then the typical subcutaneously Enbrel 50mg every 3 days, should be 25mg every 6 days subdermally.

Over 12 months, Aim 2 will again demonstrate the advantages of ASIS device injecting subdermally versus subcutaneously, but using Enbrel instead of Gadolinium on the particular skin affected by Plaque Psoriasis. Once we have shown ASIS device's consistent performance in Aim 1, then we may assume will deliver another product (Enbrel) into that bloodless space without the need to measure Enbrel's existent in that bloodless space. Using Enbrel instead of Gadolinium, we'll demonstrate the advantages of injecting subdermally over intramuscularly for the same affected skin sites in the same 60 adult subjects.

02

Conditions studied

  • Plaque Psoriasis.

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Keywords

  • Plaque Psoriasis.
  • Subdermal bloodless space
  • Subdermal injection
  • Subcutaneous injection
  • Injectable electromyography needle
  • Electrical stimulation
  • MRI with Gadolinium
03

In context

Psoriasis

1,899 studies on the registry are indexed under Psoriasis; 233 are open to participants now.

This study's planned enrollment of 60 is below the median of 70 across 1,447 interventional studies indexed under Psoriasis.

Browse Psoriasis studies →

Lead sponsor

ASIS Corporation is the lead sponsor of 3 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
21 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Eligibility criteria

Inclusion Criteria:

  • Inclusion Criteria in general and for Gadolinium:
  • Main Criteria for Inclusion: Eligible Ages: 12 Years to 65
  • Genders Eligible for Study: Both
  • Accepts Healthy Volunteers: Yes
  • Must be outpatient, male or female, of any race, between 18 and 65 years of age.
  • Must be able to understand the requirements of the study including maintaining a diary, and sign informed consent.
  • Must be in good general health as determined by investigator.
  • If female of childbearing potential, must have negative pregnancy test result at screening visit and practice reliable method of contraception
  • Inclusion Criteria for Plaque Psoriasis in particular:
  • Must have chronic moderate to severe plaque psoriasis and be candidates for systemic therapy or phototherapy.
  • Must have psoriasis involving at least 10% of body surface and a minimum PASI score of 10.
  • Patients are limited to low-moderate-strength topical corticosteroids in axillary, groin, and scalp regions.

Exclusion Criteria:

  • Exclusion Criteria for Plaque Psoriasis in particular:
  • Patients with guttate, erythrodermic, or pustular psoriasis and patients with severe infections within 4 weeks of screening are excluded from study.
  • No concomitant major anti-psoriatic therapies are allowed during the study.
  • Has chronic or recurrent infection, has been exposed to tuberculosis, has resided or traveled in areas of endemic tuberculosis or endemic mycoses, such as histoplasmosis, coccidioidomycosis, or blastomycosis; or has underlying conditions that may predispose them to infection such as advanced or poorly controlled diabetes
05

Study design

Phase
Phase 1 / Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
60 participants (estimated)

Study arms

  • Experimental
    For Left Upper Arm

    For Left Upper Arm Total Persistent % subdermally, For Left Upper Arm Total Persistent % subcutaneously, and For Left Upper Arm Relative Prolongation Ability Score. Gadolinium Magnevist® (gadopentetate dimeglumine) .1cc/ diluted with .9cc normal saline subcutaneously for 30 patients, and subdermally with ASIS Device for 30 patients.

    Drug: Gadolinium

  • Experimental
    For Right Upper Arm

    For Right Upper Arm Total Persistent % subdermally, For Left Upper Arm Total Persistent % subcutaneously, and For Left Upper Arm Relative Prolongation Ability Score. Gadolinium Magnevist® (gadopentetate dimeglumine) .1cc/ diluted with .9cc normal saline subcutaneously for 30 patients, and subdermally with ASIS Device for 30 patients.

    Drug: Gadolinium

  • Experimental
    sPGA 50 n(%)

    sPGA 50 n(%) as Efficacy of Enbrel subcutaneously at Week 12, Efficacy of Enbrel subcutaneously at Week 24, and Efficacy of Enbrel subcutaneously at Week 36 vs. Efficacy of Enbrel subdermally at Week 12, Efficacy of Enbrel subdermally at Week 24, and Efficacy of Enbrel subdermally at Week 36. sPGA 50 n(%) "clear" or "minimal" is the % of patients who achieve a score of "clear" or "minimal" by the Static Physician Global Assessment (sPGA) and % of patients with a reduction of PASI of at least 50% from baseline.

    Drug: Efficacy of Enbrel subcutaneously at Week 12 · Drug: Efficacy of Enbrel subcutaneously at Week 24 · Drug: Efficacy of Enbrel subcutaneously at Week 36 · Drug: Efficacy of Enbrel subdermally at Week 12 · Drug: Efficacy of Enbrel subdermally at Week 24 · Drug: Efficacy of Enbrel subdermally at Week 36

  • Experimental
    PASI 75 n(%)

    PASI 75 n(%) Response to treatment defined as the proportion of patients who achieved a reduction in score of at least 75% from baseline by the PASI, as PASI 75 n(%) subcutaneously at Week 12, PASI 75 n(%) subcutaneously at Week 24, and PASI 75 n(%) subcutaneously at Week 36 vs. PASI 75 n(%) subdermally at Week 12, PASI 75 n(%) subdermally at Week 24, and PASI 75 n(%) subdermally at Week 36.

    Drug: PASI 75 n(%) subcutaneously at Week 12 · Drug: PASI 75 n(%) subcutaneously at Week 24 · Drug: PASI 75 n(%) subcutaneously at Week 36 · Drug: PASI 75 n(%) subdermally at Week 12 · Drug: PASI 75 n(%) subdermally at Week 24 · Drug: PASI 75 n(%) subdermally at Week 36

  • Experimental
    Adverse Injection site reactions

    Injection site reactions as Adverse Reactions of Enbrel subcutaneously vs. Adverse Reactions of Enbrel subdermally at Week 36.

    Drug: Adverse Reactions of Enbrel subcutaneously · Drug: Adverse Reactions of Enbrel subdermally at Week 36

  • Experimental
    Adverse Reactions with Heart failure

    Heart failure as Adverse Reactions of Enbrel subcutaneously vs. Adverse Reactions of Enbrel subdermally at Week 36.

    Drug: Adverse Reactions of Enbrel subcutaneously · Drug: Adverse Reactions of Enbrel subdermally at Week 36

  • Experimental
    Adverse Reactions Allergic Reactions

    Allergic Reactions as Adverse Reactions of Enbrel subcutaneously vs. Adverse Reactions of Enbrel subdermally at Week 36.

    Drug: Adverse Reactions of Enbrel subcutaneously · Drug: Adverse Reactions of Enbrel subdermally at Week 36

  • Experimental
    Adverse Reactions Blood/low blood counts

    Blood problems/low blood counts as Adverse Reactions of Enbrel subcutaneously vs. Adverse Reactions of Enbrel subdermally at Week 36.

    Drug: Adverse Reactions of Enbrel subcutaneously · Drug: Adverse Reactions of Enbrel subdermally at Week 36

  • Experimental
    Adverse Reactions with Nervous system

    Nervous system problems, such as multiple sclerosis, seizures, or inflammation of the nerves of the eyes, as Adverse Reactions of Enbrel subcutaneously vs. Adverse Reactions of Enbrel subdermally at Week 36.

    Drug: Adverse Reactions of Enbrel subcutaneously · Drug: Adverse Reactions of Enbrel subdermally at Week 36

  • Experimental
    Adverse Reactions with Infections

    Infections (upper respiratory infection, pyelonephritis, bronchitis, septic osteomyelitis, wound infection, pneumonia, foot abscess, leg ulcer), as Adverse Reactions of Enbrel subcutaneously vs. Adverse Reactions of Enbrel subdermally at Week 36.

    Drug: Adverse Reactions of Enbrel subcutaneously · Drug: Adverse Reactions of Enbrel subdermally at Week 36

  • Experimental
    Adverse Reactions with Malignancies

    Malignancies (lymphoma, basal \& squamous skin cancer, non-cutaneous solid tumor, \& Wegener's granulomatosis), as Adverse Reactions of Enbrel subcutaneously vs. Adverse Reactions of Enbrel subdermally at Week 36.

    Drug: Adverse Reactions of Enbrel subcutaneously · Drug: Adverse Reactions of Enbrel subdermally at Week 36

  • Experimental
    Adverse Reactions with Immunogenicity

    Immunogenicity as Adverse Reactions of Enbrel subcutaneously vs. Adverse Reactions of Enbrel subdermally at Week 36.

    Drug: Adverse Reactions of Enbrel subcutaneously · Drug: Adverse Reactions of Enbrel subdermally at Week 36

  • Experimental
    Adverse Reactions with Autoantibodies

    Autoantibodies, Lupus-like syndrome, autoimmune hepatitis, as Adverse Reactions of Enbrel subcutaneously vs. Adverse Reactions of Enbrel subdermally at Week 36.

    Drug: Adverse Reactions of Enbrel subcutaneously · Drug: Adverse Reactions of Enbrel subdermally at Week 36

Interventions

  • DrugGadolinium

    For Left Upper Arm Total Persistent % subdermally, on MRI at 6 hrs, 12 hrs, and 24 hrs. Gadolinium Magnevist® (gadopentetate dimeglumine) .1cc/ diluted with .9cc normal saline subcutaneously for 30 patients, and subdermally with ASIS Device for 30 patients.

    Also known as: Gadolinium Magnevist® (gadopentetate dimeglumine)

  • DrugGadolinium

    For Left Upper Arm Total Persistent % subcutaneously, on MRI at 6 hrs, 12 hrs, and 24 hrs. Gadolinium Magnevist® (gadopentetate dimeglumine) .1cc/ diluted with .9cc normal saline subcutaneously for 30 patients, and subdermally with ASIS Device for 30 patients.

    Also known as: Gadolinium Magnevist® (gadopentetate dimeglumine)

  • DrugGadolinium

    For Left Upper Arm Relative Prolongation Ability Score or total Persistent % of Gadolinium subdermally over total Persistent % of Gadolinium subcutaneously on MRI.

    Also known as: Gadolinium Magnevist® (gadopentetate dimeglumine)

  • DrugEfficacy of Enbrel subcutaneously at Week 12

    sPGA 50 n(%) as Efficacy of Enbrel subcutaneously at Week 12, in terms of Proportion of patients who achieve a score of "clear" or "minimal" by the Static Physician Global Assessment (sPGA) and the proportion of patients with a reduction of PASI of at least 50% from baseline. The sPGA is a 6-category scale ranging from "5 = severe" to "0 = none" indicating the physician's overall assessment of the psoriasis severity focusing on indurations, erythema, and scaling. Treatment success of "clear" or "minimal" consists of none or minimal elevation in plaque, up to faint red coloration in erythema, and none or minimal fine scale over \< 5% of the plaque.

    Also known as: Enbrel (etanercept)

  • DrugEfficacy of Enbrel subcutaneously at Week 24

    sPGA 50 n(%) as Efficacy of Enbrel subcutaneously at Week 24, in terms of Proportion of patients who achieve a score of "clear" or "minimal" by the Static Physician Global Assessment (sPGA) and the proportion of patients with a reduction of PASI of at least 50% from baseline. The sPGA is a 6-category scale ranging from "5 = severe" to "0 = none" indicating the physician's overall assessment of the psoriasis severity focusing on indurations, erythema, and scaling. Treatment success of "clear" or "minimal" consists of none or minimal elevation in plaque, up to faint red coloration in erythema, and none or minimal fine scale over \< 5% of the plaque.

    Also known as: Enbrel (etanercept)

  • DrugEfficacy of Enbrel subcutaneously at Week 36

    sPGA 50 n(%) as Efficacy of Enbrel subcutaneously at Week 36, in terms of Proportion of patients who achieve a score of "clear" or "minimal" by the Static Physician Global Assessment (sPGA) and the proportion of patients with a reduction of PASI of at least 50% from baseline. The sPGA is a 6-category scale ranging from "5 = severe" to "0 = none" indicating the physician's overall assessment of the psoriasis severity focusing on indurations, erythema, and scaling. Treatment success of "clear" or "minimal" consists of none or minimal elevation in plaque, up to faint red coloration in erythema, and none or minimal fine scale over \< 5% of the plaque.

    Also known as: Enbrel (etanercept)

  • DrugEfficacy of Enbrel subdermally at Week 12

    sPGA 50 n(%) as Efficacy of Enbrel subdermally at Week 12, in terms of Proportion of patients who achieve a score of "clear" or "minimal" by the Static Physician Global Assessment (sPGA) and the proportion of patients with a reduction of PASI of at least 50% from baseline. The sPGA is a 6-category scale ranging from "5 = severe" to "0 = none" indicating the physician's overall assessment of the psoriasis severity focusing on indurations, erythema, and scaling. Treatment success of "clear" or "minimal" consists of none or minimal elevation in plaque, up to faint red coloration in erythema, and none or minimal fine scale over \< 5% of the plaque.

    Also known as: Enbrel (etanercept)

  • DrugEfficacy of Enbrel subdermally at Week 24

    sPGA 50 n(%) as Efficacy of Enbrel subdermally at Week 24, in terms of Proportion of patients who achieve a score of "clear" or "minimal" by the Static Physician Global Assessment (sPGA) and the proportion of patients with a reduction of PASI of at least 50% from baseline. The sPGA is a 6-category scale ranging from "5 = severe" to "0 = none" indicating the physician's overall assessment of the psoriasis severity focusing on indurations, erythema, and scaling. Treatment success of "clear" or "minimal" consists of none or minimal elevation in plaque, up to faint red coloration in erythema, and none or minimal fine scale over \< 5% of the plaque.

    Also known as: Enbrel (etanercept)

  • DrugEfficacy of Enbrel subdermally at Week 36

    sPGA 50 n(%) as Efficacy of Enbrel subdermally at Week 36, in terms of Proportion of patients who achieve a score of "clear" or "minimal" by the Static Physician Global Assessment (sPGA) and the proportion of patients with a reduction of PASI of at least 50% from baseline. The sPGA is a 6-category scale ranging from "5 = severe" to "0 = none" indicating the physician's overall assessment of the psoriasis severity focusing on indurations, erythema, and scaling. Treatment success of "clear" or "minimal" consists of none or minimal elevation in plaque, up to faint red coloration in erythema, and none or minimal fine scale over \< 5% of the plaque.

    Also known as: Enbrel (etanercept)

  • DrugPASI 75 n(%) subcutaneously at Week 12

    PASI 75 n(%) as Efficacy of Enbrel subcutaneously at Week 12, in terms of the proportion of patients who achieved a reduction in score of at least 75% from baseline by the PASI.

    Also known as: Enbrel (etanercept)

  • DrugPASI 75 n(%) subcutaneously at Week 24

    PASI 75 n(%) as Efficacy of Enbrel subcutaneously at Week 24, in terms of the proportion of patients who achieved a reduction in score of at least 75% from baseline by the PASI.

    Also known as: Enbrel (etanercept)

  • DrugPASI 75 n(%) subcutaneously at Week 36

    PASI 75 n(%) as Efficacy of Enbrel subcutaneously at Week 36, in terms of the proportion of patients who achieved a reduction in score of at least 75% from baseline by the PASI.

    Also known as: Enbrel (etanercept)

  • DrugPASI 75 n(%) subdermally at Week 12

    PASI 75 n(%) as Efficacy of Enbrel subdermally at Week 12, in terms of the proportion of patients who achieved a reduction in score of at least 75% from baseline by the PASI.

    Also known as: Enbrel (etanercept)

  • DrugPASI 75 n(%) subdermally at Week 24

    PASI 75 n(%) as Efficacy of Enbrel subdermally at Week 24, in terms of the proportion of patients who achieved a reduction in score of at least 75% from baseline by the PASI.

    Also known as: Enbrel (etanercept)

  • DrugPASI 75 n(%) subdermally at Week 36

    PASI 75 n(%) as Efficacy of Enbrel subdermally at Week 36, in terms of the proportion of patients who achieved a reduction in score of at least 75% from baseline by the PASI.

    Also known as: Enbrel (etanercept)

  • DrugAdverse Reactions of Enbrel subcutaneously

    Adverse Reactions of Enbrel subcutaneously at Week 36, in number of Injection site reactions, Heart failure, Allergic Reactions, Blood problems/low blood counts, Nervous system, Infections, Malignancies, Immunogenicity, and Autoantibodies.

    Also known as: Enbrel (etanercept)

  • DrugAdverse Reactions of Enbrel subdermally at Week 36

    Adverse Reactions of Enbrel subdermally at Week 36, in number of Injection site reactions, Heart failure, Allergic Reactions, Blood problems/low blood counts, Nervous system, Infections, Malignancies, Immunogenicity, and Autoantibodies.

    Also known as: Enbrel (etanercept)

  • DrugGadolinium

    For Right Upper Arm Total Persistent % subdermally, on MRI at 6 hrs, 12 hrs, and 24 hrs. Gadolinium Magnevist® (gadopentetate dimeglumine) .1cc/ diluted with .9cc normal saline subcutaneously for 30 patients, and subdermally with ASIS Device for 30 patients.

    Also known as: Gadolinium Magnevist® (gadopentetate dimeglumine)

  • DrugGadolinium

    For Right Upper Arm Total Persistent % subcutaneously, on MRI at 6 hrs, 12 hrs, and 24 hrs. Gadolinium Magnevist® (gadopentetate dimeglumine) .1cc/ diluted with .9cc normal saline subcutaneously for 30 patients, and subdermally with ASIS Device for 30 patients.

    Also known as: Gadolinium Magnevist® (gadopentetate dimeglumine)

  • DrugGadolinium

    For Right Upper Arm Relative Prolongation Ability Score or total Persistent % of Gadolinium subdermally over total Persistent % of Gadolinium subcutaneously on MRI.

    Also known as: Gadolinium Magnevist® (gadopentetate dimeglumine)

06

What researchers measure

Primary outcomes

  1. Relative Prolongation Ability Score for Gadolinium subdermally injected.

    Gadolinium will be injected with ASIS subdermally (30) or conventional subcutaneous (30) for 60 adult subjects with Plaque Psoriasis (involving at least 10% of body surface and a minimum Psoriasis Area \& Severity Index (PASI) score of 10), just for the particular plaque skin area. The first MRI taken promptly after Gadolinium injection for each patient would be his or her reference of 100% Persistent, to which his or her subsequent MRI taken @ 6 hr, @ 12 hr, and @24hr later will be compared for Persistent %.This approximation can only work if the variables are minimized to the same population with Plaque Psoriasis, and the particular plaque skin area. The Relative Prolongation Ability Score or total Persistent % subdermally over total Persistent % subcutaneously, Plaque Psoriasis will be very valuable indicators for us to modify the Enbrel dosage and duration for testing with that "unknown" subdermal bloodless space in Aim 2.

    Time frame: 6 months

Secondary outcomes

  1. Efficacy of Enbrel subcutaneously vs. subdermally in Plaque Psoriasis.

    Hypothetically, if that subdermal bloodless space in patients somehow failed to show prolongation of half-life for Gadolinium in Aim 1, we can still proceed with Aim 2, because Enbrel's Pharmacokinetics will be studied anyway, by following tumor necrosis factor, then comparing the Mean tumor necrosis factor receptor : Fc. However, the Pharmacokinetics of subdermally injected Enbrel will be just dependent on Enbrel's diffusion out of that subdermal bloodless space. Therefore, if Enbrel getting into the bloodstream becomes so severely inhibited, then we can just change the osmolality of Enbrel in the end. Response to treatment will be assessed after 3, 6 and 9 months of therapy, and defined as the patients who achieved a reduction in score of at least 75% from baseline by the PASI.8 Other therapeutic advantages of ASIS device subdermally over subcutaneously will also be studied by comparing the reduction of adverse reactions and injection site pain.

    Time frame: 12 months

Other outcomes

  1. Adverse Reactions of Enbrel subcutaneously vs. subdermally in Plaque Psoriasis

    Adverse Reactions of Enbrel subcutaneously vs. subdermally: Heart failure, Allergic Reactions, Blood problems/low blood counts, Nervous system problems, such as multiple sclerosis, seizures, or inflammation of the nerves of the eyes, Infections (upper respiratory infection, pyelonephritis, bronchitis, septic osteomyelitis, wound infection, pneumonia, foot abscess, leg ulcer), Malignancies (lymphoma, basal \& squamous skin cancer, non-cutaneous solid tumor, \& Wegener's granulomatosis), Immunogenicity, Autoantibodies, Lupus-like syndrome, autoimmune hepatitis, and Injection site pain.

    Time frame: 12 months

07

Study locations

2 sites
  • Automatic Subdermal Injector System, Inc
    Westminster, California 92683, United States
  • Automatic Subdermal Injector System, Inc
    Westminster, California 92683, United States
08

References and documents

Publications

  • Fisher CJ Jr, Agosti JM, Opal SM, Lowry SF, Balk RA, Sadoff JC, Abraham E, Schein RM, Benjamin E. Treatment of septic shock with the tumor necrosis factor receptor:Fc fusion protein. The Soluble TNF Receptor Sepsis Study Group. N Engl J Med. 1996 Jun 27;334(26):1697-702. doi: 10.1056/NEJM199606273342603. PubMed 8637514 ↗
  • Ware JE Jr, Gandek B. Overview of the SF-36 Health Survey and the International Quality of Life Assessment (IQOLA) Project. J Clin Epidemiol. 1998 Nov;51(11):903-12. doi: 10.1016/s0895-4356(98)00081-x. PubMed 9817107 ↗
  • Bhutani T, Wong JW, Bebo BF, Armstrong AW. Access to health care in patients with psoriasis and psoriatic arthritis: data from National Psoriasis Foundation survey panels. JAMA Dermatol. 2013 Jun;149(6):717-21. doi: 10.1001/jamadermatol.2013.133. PubMed 23783152 ↗
  • Paonessa DF, Goldstein JC. Anatomy and physiology of head and neck infections (with emphasis on the fascia of the face and neck). Otolaryngol Clin North Am. 1976 Oct;9(3):561-80. No abstract available. PubMed 980495 ↗
  • Ramey DR, Fries JF, Singh G. The Health Assessment Questionnaire 1995 - Status and Review. In: Spilker B, ed. "Quality of Life and Pharmacoeconomics in Clinical Trials." 2nd ed. Philadelphia, PA. Lippincott-Raven 1996;227
  • Enbrel (etanercept) Product Information http://pi.amgen.com/united_states/enbrel/derm/enbrel_pi
  • GAMMAGARD LIQUID Comparison of Intravenous and Subcutaneous Administration in Primary Immunodeficiency Diseases (PID). http://www.clinicaltrials.gov/ct2/show/NCT00546871?term=Gammagard+subcutaneous&rank=5
  • Magnevist (gadopentetate dimeglumine) Injection Product Information. http://bayerimaging.com/products/magnevist/safety-information_nsf.php
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 24, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02112097
Lead sponsor
ASIS Corporation
Responsible party
Sponsor
First posted
Apr 11, 2014
Start date
Jan 2016
Primary completion
Jun 2016 (estimated)
Completion
Jun 2017 (estimated)
Last update
Jun 24, 2015

Study contacts

Li Nguyen, MD
Contact
dr.li.nguyen@asis-inc.com
(714)-453-7857
Thanh Phung, MD
Contact
thanhphung@idit-inc.com
714-893-1915
Li Nguyen, MD
principal investigator · AUTOMATIC SUBDERMAL INJECTOR SYSTEM INC
Thanh Phung,, MD
principal investigator · AUTOMATIC SUBDERMAL INJECTOR SYSTEM, INC

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

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