Vgx 3100 phase 3 results

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Sep 30, 2020 · Specifically, INOVIO's lead candidate VGX-3100, currently in Phase 3 trials for precancerous cervical dysplasia, destroyed and cleared high-risk HPV 16 and 18 in a Phase 2b clinical trial

The final results, says Chikere will “help elucidate the clinical profile of Dec 14, 2021 · The second global phase 3 clinical trial of VGX-3100 for cervical HSIL is fully enrolled and top-line efficacy and safety data are expected to be available in the second half of 2022 Dec 14, 2021 · Separately, INOVIO partner Apollo Bio has become the first participant in the VGX-3100 Phase 3 clinical trial . inovio highlights key updates on phase 3 program for vgx-3100 VGX-3100 has the What is the VGX-3100 trial? This trial is one of two ongoing pivotal, randomized, double-blind, multi-center, placebo-controlled, Phase 3 trials (REVEAL 1 and REVEAL 2) evaluating the safety, tolerability and efficacy of VGX-3100 to treat HPV-16/18-associated cervical high-grade squamous intraepithelial lesions (HSIL) using the company's proprietary CELLECTRA® 5PSP device .

INOVIO is in open-label Phase 2 clinical trials evaluating its ecacy for treating HPV-related vulvar and anal dysplasia (HSIL) A Prospective, Randomized, Double-Blind, Placebo-Controlled Phase 3 Study of VGX-3100 Delivered Intramuscularly Followed by Electroporation With CELLECTRA-5PSP for the Treatment of HPV-16 and/or HPV-18 Related High Grade Squamous Intraepithelial Lesion (HSIL) of the Cervix Specifically, INOVIO’s lead candidate VGX-3100 is the first DNA medicine to achieve efficacy endpoints in a Phase 3 clinical trial, REVEAL 1, for the treatment of precancerous cervical dysplasia caused by HPV-16 and/or HPV-18 . VGX-3100 is designed to utilize the patient's own immune system to Dec 14, 2021 · INOVIO's lead immunotherapy candidate, VGX-3100, currently in Phase 3 trials for precancerous cervical dysplasia, cleared high-risk HPV-16 and/or HPV-18 in a Phase 2b clinical trial Nov 17, 2021 · INOVIO has completed follow-up of subjects in REVEAL 1 (Randomized Evaluation of VGX-3100 and Electroporation for the treatment of Cervical HSIL), a Phase 3 pivotal trial evaluating VGX-3100 for the treatment of cervical high-grade squamous intraepithelial lesions caused by HPV-16 and/or HPV-18, for safety and durability of virological Mar 26, 2020 · About VGX-3100 VGX-3100 is a DNA medicine under Phase 3 investigation for the treatment of HPV-16 and HPV-18 infection and precancerous lesions of the cervix .

VGX-3100 is a DNA-based immunotherapy under investigation for the treatment of HPV 16 and HPV 18 infection and precancerous lesions of the cervix (Phase 3) and vulva and anus (Phase 2)

Dec 09, 2020 · The open label, single arm trial also showed VGX-3100 to be safe and well-tolerated in treating men and women with HPV-16-/18-associated anal dysplasia Specifically, INOVIO’s lead candidate VGX-3100, currently in Phase 3 trials for precancerous cervical dysplasia, destroyed and cleared high-risk HPV 16 and 18 in a Phase 2b clinical trial . Mar 01, 2021 · INOVIO Announces Positive Results from REVEAL 1, a Phase 3 Pivotal Trial Evaluating VGX-3100, its DNA-based HPV Immunotherapy for the Treatment of High-grade Precancerous Read this content Click here to read the original version at the source's official website placebo group •Immunization with VGX-3100 results in regression of CIN2/3 to CIN1 or normal and virological clearance of HPV 16 and/or 18 Jan 06, 2021 · A Phase 2 trial of VGX-3100 in the treatment of anal HSIL was also conducted with positive efficacy results 3 .

VGX-3100 has the potential to be the rst approved treatment Mar 01, 2021 · About VGX-3100

dosing for innovate phase 3 segment is underway and been previously reported for VGX-3100 from a Phase 2b ran-domized, placebo-controlled, double-blind clinical trial 20 With the addition of recombinant cytokine IL-12 to this HPV DNA vaccine, MEDI0457 is anticipated to boost Nov 09, 2021 · Specifically, INOVIO's lead therapeutic candidate VGX-3100 met primary and secondary endpoints for all evaluable subjects in REVEAL 1, the first of two, Phase 3 trials for precancerous cervical Nov 09, 2021 · Specifically, INOVIO’s leading drug candidate VGX-3100 was the first REVEAL 1 of two Phase 3 trials of precancerous cervical dysplasia, the primary and secondary of all evaluable subjects . Jun 08, 2017 · VGX-3100 is a DNA-based immunotherapy under investigation for the treatment of HPV-16 and HPV-18 infection and pre-cancerous lesions of the cervix (phase 3) and vulva (phase 2) Mar 03, 2021 · INOVIO Announces Positive Results from REVEAL 1, a Phase 3 Pivotal Trial Evaluating VGX-3100, its DNA-based HPV Immunotherapy for the Treatment of High-grade Precancerous Cervical Dysplasia Caused by HPV-16 and/or HPV-18 .

In 2018, the two companies signed an agreement giving Apollo Bio the Mar 02, 2021 · INOVIO president and CEO Dr J Joseph Kim said: “INOVIO is very proud to advance VGX-3100 as the first DNA medicine to achieve efficacy endpoints in a Phase III clinical trial in all evaluable subjects

March 3, 2021 by admin 0 Comments Mar 10, 2021 · About VGX-3100 Aug 15, 2018 · VGX-3100 demonstrated in a phase 2b study its ability to clear HPV-16 and HPV-18 infection and pre-cancerous lesions . High-risk HPV About VGX-3100 VGX-3100 is a DNA medicine in clinical trials for the treatment of three HPV-16-/18-related disease states – cervical dysplasia, vulvar dysplasia and anal dysplasia 's VGX-3100 met its primary and secondary endpoints in a phase 3 trial to treat HPV-16/18-associated cervical high-grade squamous intraepithelial lesions (HSIL) .

Mar 01, 2021 · INOVIO's lead immunotherapy candidate, VGX-3100, currently in Phase 3 trials for precancerous cervical dysplasia, cleared high-risk HPV-16 and/or HPV-18 in a Phase 2b clinical trial

Sep 23, 2021 · INOVIO Highlights Key Updates on Phase 3 Program for VGX-3100, its DNA-based Immunotherapy for the Treatment of Cervical HSIL Caused by HPV-16 and/or HPV-18 PR Newswire (US) - 12/14/2021 8:00:00 AM INOVIO starting development of Omicron-specific COVID vaccine candidate Seeking Alpha - 11/30/2021 9:03:04 AM inovio highlights key updates on phase 3 program for vgx-3100 Dec 15, 2021 · Clinical Trial NCT03185013: Phase 3 Clinical Trial REVEAL 1 Evaluation of VGX-3100 and Electroporation for the Treatment of Cervical HSIL . A Prospective, Randomized, Double-Blind, Placebo-Controlled Phase 3 Study of VGX-3100 Delivered Intramuscularly Followed by Electroporation With CELLECTRA-5PSP for the Treatment of HPV-16 and/or HPV-18 Related High Grade Squamous Intraepithelial Lesion (HSIL) of the Cervix What is the VGX-3100 trial? This trial is one of two ongoing pivotal, randomized, double-blind, multi-center, placebo-controlled, Phase 3 trials (REVEAL 1 and REVEAL 2) evaluating the safety, tolerability and efficacy of VGX-3100 to treat HPV-16/18-associated cervical high-grade squamous intraepithelial lesions (HSIL) using the company's proprietary CELLECTRA® 5PSP device The cervical dysplasia program is in late Phase 3 clinical trials (REVEAL 1 and REVEAL 2) .

Feb 24, 2021 · Specifically, INOVIO's lead candidate VGX-3100, currently in Phase 3 trials for precancerous cervical dysplasia, destroyed and cleared high-risk HPV 16 and 18 in a Phase 2b clinical trial

INO Inovio Pharmaceuticals Inc New INOVIO Highlights Key Updates on Phase 3 Program for VGX-3100, its DNA-based Immunotherapy for the Treatment of Cervical HSIL Caused by HPV-16 and/or HPV-18 The most common side effect was injection site pain, and no serious adverse events were reported inovio reports third quarter 2021 financial results . Patients from 36 academic and private gynaecology practices in seven countries were randomised (3:1) to receive 6 mg VGX-3100 or placebo (1 mL), given intramuscularly at 0 Brief Title: REVEAL 1 (Evaluation of VGX-3100 and Electroporation for the Treatment of Cervical HSIL) Official Title: A Prospective, Randomized, Double-Blind, Placebo-Controlled Phase 3 Study of VGX-3100 Delivered Intramuscularly Followed by Electroporation With CELLECTRA™-5PSP for the Treatment of HPV-16 and/or HPV-18 Related High Grade Squamous Intraepithelial Lesion (HSIL) of the Cervix Feb 24, 2021 · Specifically, INOVIO’s lead candidate VGX-3100, currently in Phase 3 trials for precancerous cervical dysplasia, destroyed and cleared high-risk HPV 16 and 18 in a Phase 2b clinical trial The trial is expected to enroll up to 84 participants .

regulator “has placed a clinical hold on its proposed Phase III clinical program for VGX-3100,” with the FDA apparently concerned about the shelf-life Dec 14, 2021 · INOVIO issued updates on the phase 3 program for VGX-3100 for HPV-associated cervical high-grade squamous intraepithelial lesions

Phase 3 study China The design is similar to REVEAL 1 and REVEAL 2-randomized, double-blind, placebo-controlled VGX-3100 is a DNA medicine in clinical trials for the treatment of three HPV-16/18 related disease Sep 17, 2015 · Efficacy, safety, and immunogenicity of VGX-3100 were assessed in CIN2/3 associated with HPV-16 and HPV-18, in a randomised, double-blind, placebo-controlled phase 2b study . High-risk HPV is responsible for 70% of cervical cancer, 91% of anal cancer, and 69% of vulvar cancer Jan 26, 2022 · Positive phase 2 glioblastoma results could also be a catalyst for a higher stock price .

This trial is being run by ApolloBio and is similar in design to REVEAL2

Oct 26, 2016 · The company was looking to move VGX-3100 into phase III development in the fourth quarter but with the clinical hold in place, the company is now expecting that the program will be delayed until VGX-3100 for the Treatment of HPV16/18 Related Cervical HSIL: Results from a Phase 3 Study (Abstract #233) Results of VGX-3100 for the Treatment of HPV16/18 Associated Vulvar HSIL: Phase 2 Open-Label Trial Efficacy and Safety Results (Abstract #164) Apr 05, 2021 · In an earlier phase 1 pilot study (NCT00685412), women with HPV-16/HPV-18–positive high-grade cervical intraepithelial neoplasia received VGX-3100 alone, which induced E6/E7-specific immune responses and a 50% rate of tumor regression Aug 04, 2021 · The VGX-3100 is currently in Phase 3 clinical trials . or Inovio Completes Enrollment of VGX-3100 Phase 3 Trial (REVEAL 1) for the Treatment of HPV-Related Cervical Pre-cancer REVEAL 1 Phase 3 clinical trial for VGX-3100 met primary and secondary endpoints among all evaluable subjects .

Oct 15, 2012 · Inovio's VGX-3100 is designed to raise immune responses against the E6 and E7 oncogenes associated with HPV types 16 and 18, i

” “INOVIO recognizes and applauds the incredible work to address the global COVID-19 pandemic across the industry, while also Inovio Pharmaceutical Inc Apr 23, 2021 · Specifically, INOVIO's lead candidate VGX-3100 is the first DNA medicine to achieve efficacy endpoints in a Phase 3 clinical trial, REVEAL 1, for the treatment of precancerous cervical dysplasia Nov 17, 2021 · INOVIO has completed follow-up of subjects in REVEAL 1 (Randomized Evaluation of VGX-3100 and Electroporation for the treatment of Cervical HSIL), a Phase 3 pivotal trial evaluating VGX-3100 for the treatment of cervical high-grade squamous intraepithelial lesions caused by HPV-16 and/or HPV-18, for safety and durability of virological About VGX-3100 . 13, 14 In a phase 1 trial in women in whom CIN2/3 lesions had been resected, intramuscular injection of VGX Jun 14, 2017 · Phase 3 Trial for Inovio's VGX-3100 in Cervical Dysplasia Gets FDA Go-Ahead Source: The Life Sciences Report (6/14/17) Now that the FDA has lifted its clinical hold on Phase 3 study of Inovio Pharmaceutical's immunotherapy for cervical dysplasia, three analysts are making note of what the progress means for both the company and investors The cervical dysplasia program is in late Phase 3 clinical trials 3 Mar 01, 2021 · Inovio Pharmaceuticals, Inc .

The Phase 3 trial in China is similar in design to REVEAL1 and REVEAL2 – randomized, double-blinded, placebo-controlled

Patient characteristics observed at study entry showed that 80% of the population had vulval intraepithelial neoplasia (VIN) 3 disease, and 88% showed a history of at least 1 recurrence • VGX-3100 is generally well-tolerated with only administration site redness occurring significantly more frequently in the VGX-3100 group vs . The REVEAL studies are prospective, randomized, double-blind, placebo-controlled trials evaluating adult women with HPV-16 Dec 14, 2021 · INOVIO issued updates on the phase 3 program for VGX-3100 for HPV-associated cervical high-grade squamous intraepithelial lesions Additionally, two out of four metastatic HPV-associated head and neck cancer patients treated with MEDI0457 and a PD-1 check point inhibitors in a Phase 1 trial experienced a long-term complete response for more two years and counting Oct 13, 2021 · Phase 3 Trial for Inovio's VGX-3100 in Cervical Dysplasia Gets FDA Go-Ahead Source: The Life Sciences Report (6/14/17) Now that the FDA has lifted its clinical hold on Phase 3 study of Inovio Pharmaceutical's immunotherapy for cervical dysplasia, three analysts are making note of what the progress means for both the company and investors .

Inovio Pharmaceuticals Stock Chart Inovio also has potential drugs or vaccines for several forms of cancer, Ebola, HIV and more, although most are still in the early stages of development

High Mar 02, 2021 · If VGX-3100 turns out to be another dud, Inovio's Covid-19 vaccine candidate INO-4800 looks unlikely to save the company Apr 23, 2021 · Specifically, INOVIO's lead candidate VGX-3100 is the first DNA medicine to achieve efficacy endpoints in a Phase 3 clinical trial, REVEAL 1, for the treatment of precancerous cervical dysplasia What is the VGX-3100 trial? This trial is one of two ongoing pivotal, randomized, double-blind, multi-center, placebo-controlled, Phase 3 trials (REVEAL 1 and REVEAL 2) evaluating the safety, tolerability and efficacy of VGX-3100 to treat HPV-16/18-associated cervical high-grade squamous intraepithelial lesions (HSIL) using the company's proprietary CELLECTRA® 5PSP device . Heavy reliance on partners for funds to develop its pipeline candidates is a persistent concern The clinical trial for cervical precancerous lesions has obtained the first positive results of phase III clinical trials in the United States .

There is a risk that the results of the second phase 3 VGX-3100 study will not be positive, or that the FDA will find a reason to reject the vaccine, or that the market for the vaccine will be smaller than I expect The second global phase 3 clinical trial of VGX-3100 for cervical HSIL is fully enrolled and top-line efficacy and safety data are expected to be available in the second half of 2022 . Mar 31, 2021 · INOVIO Announces Positive Results from REVEAL 1, a Phase 3 Pivotal Trial Evaluating VGX-3100, its DNA-based HPV Immunotherapy for the Treatment of High-grade Precancerous Cervical Dysplasia Caused by Mar 01, 2021 · INOVIO Announces Positive Results from REVEAL 1, a Phase 3 Pivotal Trial Evaluating VGX-3100, its DNA-based HPV Immunotherapy for the Treatment of High-grade Precancerous Cervical Dysplasia Caused by HPV-16 and/or HPV-18 Dec 14, 2021 · - Phase 3 Trial in China – The first participant has been dosed in the Phase 3 trial of VGX-3100 for cervical HSIL in China The pivotal portion of that project’s phase II/III trial is still on clinical hold, and the group does not expect to start enrolling patients until late in the second quarter, by which time existing vaccines should be Jun 30, 2021 · Inovio is currently testing VGX-3100 in a second “nearly identical” Phase 3 study, with data expected next year .

Separately, INOVIO's partner ApolloBio dosed the first participant in the Phase 3 clinical trial of VGX-3100 in China

Mar 18, 2019 · Inovio's (INO) most advanced candidate, VGX-3100 vaccine, is advancing well About VGX-3100 VGX-3100 is a DNA medicine under Phase 3 investigation for the treatment of HPV-16 and HPV-18 infection and precancerous lesions of the cervix . Keep tabs on your portfolio, search for stocks, commodities, or mutual funds with screeners, customizable chart indicators and technical analysis INOVIO Announces Positive Results from REVEAL 1, a Phase 3 Pivotal Trial Evaluating VGX-3100, Its DNAbased HPV Immunotherapy for the Treatment of High-Grade Precancerous Cervical Dysplasia Caused by HPV-16 and/or HPV-18 .

Dec 14, 2021 · - Phase 3 Trial in China – The first participant has been dosed in the Phase 3 trial of VGX-3100 for cervical HSIL in China

Mar 31, 2021 · INOVIO Announces Positive Results from REVEAL 1, a Phase 3 Pivotal Trial Evaluating VGX-3100, its DNA-based HPV Immunotherapy for the Treatment of High-grade Precancerous Cervical Dysplasia Caused by Dec 14, 2021 · - Phase 3 Trial in China – The first participant has been dosed in the Phase 3 trial of VGX-3100 for cervical HSIL in China REVEAL 1 is designed to provide one-year safety data for a minimum of 198 patients on VGX-3100—the last Update Posted: February 3, 2021 . Feb 10, 2021 · HPV-301 is a prospective, randomized, double-blind, placebo controlled Phase 3 study to determine the efficacy, safety, and tolerability of VGX-3100 administered by intramuscular (IM) injection followed by electroporation (EP) delivered with CELLECTRA 5PSP in adult women with histologically confirmed cervical high grade squamous intraepithelial lesion (HSIL) (cervical intraepithelial neoplasia What is the VGX-3100 trial? This trial is one of two ongoing pivotal, randomized, double-blind, multi-center, placebo-controlled, Phase 3 trials (REVEAL 1 and REVEAL 2) evaluating the safety, tolerability and efficacy of VGX-3100 to treat HPV-16/18-associated cervical high-grade squamous intraepithelial lesions (HSIL) using the company's proprietary CELLECTRA® 5PSP device Nov 21, 2015 · VGX-3100 consists of two DNA plasmids encoding optimised synthetic consensus E6 and E7 genes of HPV-16 and HPV-18, using a proprietary design strategy, SynCon (Inovio Pharmaceuticals, Plymouth Meeting, PA, USA), as described previously .

Jan 22, 2022 · - Phase 3 Trial in China - The first participant has been dosed in the Phase 3 trial of VGX-3100 for cervical HSIL in China

INOVIO's Phase 3 program in cervical HSIL is assessing the efficacy of VGX-3100 to regress cervical HSIL, a direct precursor to cervical cancer, and to eliminate the HPV-16 and/or HPV-18 infection that causes these lesions Feb 24, 2021 · Specifically, INOVIO’s lead candidate VGX-3100, currently in Phase 3 trials for precancerous cervical dysplasia, destroyed and cleared high-risk HPV 16 and 18 in a Phase 2b clinical trial . Mark Bagarazzi, Inovio’s Chief Medical Officer, said, “VGX-3100 has the potential to be a first-in-class HPV-specific immunotherapy offering women the prospect of preventing cervical cancer without undergoing an invasive What is the VGX-3100 trial? This trial is one of two ongoing pivotal, randomized, double-blind, multi-center, placebo-controlled, Phase 3 trials (REVEAL 1 and REVEAL 2) evaluating the safety, tolerability and efficacy of VGX-3100 to treat HPV-16/18-associated cervical high-grade squamous intraepithelial lesions (HSIL) using the company's proprietary CELLECTRA® 5PSP device HPV-303 is a prospective, randomized, double-blind, placebo-controlled phase 3 study of VGX-3100 delivered intramuscularly (IM) followed by electroporation (EP) delivered with CELLECTRA™ 5PSP in adult women with histologically confirmed high-grade squamous intraepithelial lesions (HSIL) (cervical intraepithelial neoplasia grade 2 CIN2 or grade 3 CIN3) of the cervix, associated with HPV Mar 26, 2020 · About VGX-3100 VGX-3100 is a DNA medicine under Phase 3 investigation for the treatment of HPV-16 and HPV-18 infection and precancerous lesions of the cervix .

3 From that trial, in the mITT population, concomitant histopatholo-gical regression and virologic clearance occurred in 40% (46/ 114) of the VGX-3100 recipients and 15% (6/40) of the placebo Jan 22, 2022 · - Phase 3 Trial in China - The first participant has been dosed in the Phase 3 trial of VGX-3100 for cervical HSIL in China

High-risk HPV Dec 14, 2021 · The second global phase 3 clinical trial of VGX-3100 for cervical HSIL is fully enrolled and top-line efficacy and safety data are expected to be available in the second half of 2022 is the leading provider of real-time or delayed intraday stock and commodities charts and quotes . INOVIO Announces Positive Results from REVEAL 1, a Phase 3 Pivotal Trial Evaluating VGX-3100, its DNA-based HPV Immunotherapy for the Treatment of High-grade Precancerous Cervical Dysplasia Caused by HPV-16 and/or HPV-18 3/1/2021 Trial achieved primary and secondary ecacy endpoints among all evaluable subjects in the Phase 3 multi-center, Nov 19, 2021 · VGX-3100 is a synthetic DNA HPV16/18-specific immunotherapy encoding HPV-16/18 E6 and E7 proteins and is being assessed for cervical HSIL treatment efficacy and safety in two multi-national, randomized, placebo controlled phase 3 studies VGX-3100 is a DNA-based immunotherapy developed for HPV infection of the cervix and as the first non-surgical treatment for precancerous cervical lesions .

Jun 01, 2021 · INOVIO said that based upon these results, it plans to pursue Phase 3 development of VGX-3100 What is the VGX-3100 trial? This trial is one of two ongoing pivotal, randomized, double-blind, multi-center, placebo-controlled, Phase 3 trials (REVEAL 1 and REVEAL 2) evaluating the safety, tolerability and efficacy of VGX-3100 to treat HPV-16/18-associated cervical high-grade squamous intraepithelial lesions (HSIL) using the company's proprietary CELLECTRA® 5PSP device . VGX-3100 is INOVIO’s DNA medicine in clinical trials for the treatment of three HPV-16/18 related disease states – anal dysplasia, vulvar dysplasia, and cervical dysplasia Jun 14, 2017 · Phase 3 Trial for Inovio's VGX-3100 in Cervical Dysplasia Gets FDA Go-Ahead Source: The Life Sciences Report (6/14/17) Now that the FDA has lifted its clinical hold on Phase 3 study of Inovio Pharmaceutical's immunotherapy for cervical dysplasia, three analysts are making note of what the progress means for both the company and investors .

INOVIO plans to pursue a registrational Phase 3 clinical trial for HPV-16-/18-associated anal dysplasia as well as to apply for rare and orphan disease designation for this indication in 2021

VGX-3100 is a DNA medicine in clinical trials for the treatment of three HPV-16-/18-related disease states – cervical dysplasia, vulvar dysplasia and anal dysplasia INOVIO is in open-label Phase 2 clinical trials evaluating its efficacy for treating HPV-related vulvar and anal dysplasia (HSIL) . In addition to treating cervical dysplasia, label expansion is likely Feb 01, 2021 · On Tuesday, Inovio provided an update from the development of the Phase 3 program for VGX-3100, indicated to treat HPV-associated cervical high-grade squamous intraepithelial le In a little over two weeks, the curtain will close on what should go down as another winning year for the stock market .

High-grade cervical lesions and their underlying high-risk HPV-16 / 18 that meet the criteria

VGX-3100 has the potential to be the first approved treatment for HPV infection of the cervix and the first non-surgical treatment for What is the VGX-3100 trial? This trial is one of two ongoing pivotal, randomized, double-blind, multi-center, placebo-controlled, Phase 3 trials (REVEAL 1 and REVEAL 2) evaluating the safety, tolerability and efficacy of VGX-3100 to treat HPV-16/18-associated cervical high-grade squamous intraepithelial lesions (HSIL) using the company's proprietary CELLECTRA® 5PSP device We are truly proud to advance VGX-3100 as the first DNA medicine to reach this important milestone . Mar 02, 2021 · INOVIO president and CEO Dr J Joseph Kim said: “INOVIO is very proud to advance VGX-3100 as the first DNA medicine to achieve efficacy endpoints in a Phase III clinical trial in all evaluable subjects Mar 01, 2021 · INOVIO Announces Positive Results from REVEAL 1, a Phase 3 Pivotal Trial Evaluating VGX-3100, its DNA-based HPV Immunotherapy for the Treatment of High-grade Precancerous Cervical Dysplasia Caused Mar 01, 2021 · About VGX-3100 .

Jan 06, 2021 · The phase 2 study of VGX-3100 included 24 female patients aged 22 to 70 years without comorbidities VGX-3100 is the world's first therapeutic drug for HPV 16/18 infection-related precancerous lesions . Oct 26, 2016 · The company was looking to move VGX-3100 into phase III development in the fourth quarter but with the clinical hold in place, the company is now expecting that the program will be delayed until Nov 09, 2021 · Specifically, INOVIO's lead therapeutic candidate VGX-3100 met primary and secondary endpoints for all evaluable subjects in REVEAL 1, the first of two, Phase 3 trials for precancerous cervical Apr 23, 2021 · Specifically, INOVIO's lead candidate VGX-3100 is the first DNA medicine to achieve efficacy endpoints in a Phase 3 clinical trial, REVEAL 1, for the treatment of precancerous cervical dysplasia What is the VGX-3100 trial? This trial is one of two ongoing pivotal, randomized, double-blind, multi-center, placebo-controlled, Phase 3 trials (REVEAL 1 and REVEAL 2) evaluating the safety, tolerability and efficacy of VGX-3100 to treat HPV-16/18-associated cervical high-grade squamous intraepithelial lesions (HSIL) using the company's proprietary CELLECTRA® 5PSP device These oncogenes are responsible for Nov 15, 2021 · VGX-3100 for the Treatment of HPV16/18 Related Cervical HSIL: Results from a Phase 3 Study (Abstract #233) Results of VGX-3100 for the Treatment of HPV16/18 Associated Vulvar HSIL: Phase 2 Open Oct 24, 2016 · In a brief update, Inovio said the U .

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