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Endonovo Therapeutics, Inc. (ENDV)

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Previous Close0.0647
Open0.0591
Bid0.0000 x 0
Ask0.0000 x 0
Day's Range0.0501 - 0.0650
52 Week Range0.0140 - 4.0000
Volume220,141
Avg. Volume71,492
Market Cap1.139M
Beta (5Y Monthly)N/A
PE Ratio (TTM)N/A
EPS (TTM)-1.2340
Earnings DateMay 04, 2020
Forward Dividend & YieldN/A (N/A)
Ex-Dividend DateN/A
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  • GlobeNewswire

    Endonovo Therapeutics’ Offers FDA Cleared Solution to Opioid Epidemic Which Has Significantly Increased During the COVID Pandemic.

    LOS ANGELES, Oct. 08, 2020 (GLOBE NEWSWIRE) -- Endonovo Therapeutics, Inc. (OTCQB: ENDV) ("Endonovo" or the "Company"), announced today a new marketing and public awareness campaign around their FDA Cleared SofPulse® that has been proven to help the in the response to the opioid epidemic during the COVID pandemic. “Our country and the world is currently going through a very trying time due to COVID-19 which has significantly exacerbated the opioid epidemic within the U.S.. SofPulse® has shown proven clinical and surgical results - and can be a major solution to helping resolve the opioid epidemic by decreasing patient opioid abuse after patient surgeries.” stated Alan Collier CEO of Endonovo. As reported in The American Medical Association's (AMA) Advocacy Resource Center the alarming trend, showing “Increases in opioid related overdose and other concerns during COVID pandemic.” A recent Pharmacy Times interview entitled “Management Solutions for Opioid Epidemic Are Similar to Management of the COVID-19 Pandemic”, emphasized, “prevention on a public health scale is vital to addressing the COVID-19 pandemic, likewise, preventing exposure to opioids by reducing patients’ opioid requirements is the parallel achievement with regard to the opioid epidemic. A public health scale application of opioid exposure prevention would necessitate the addition of treatments to standards of care across healthcare and would be required to combat the epidemic.”Finding solutions for reducing patient opioid use after medical procedures would offer a significant solution to help overcome the opioid epidemic. The U.S. Drug Enforcement Agency (DEA) states, “80% of people who use heroin first misused prescription opioids.” Often, U.S. patients’ first exposure to opioids happens during post-surgical pain management.Alan Collier, Endonovo CEO, states, “SofPulse® device has shown in clinical and surgical trials as we have undertaken to significantly reduce patient opioid use and pain symptoms experienced post-operatively. Endonovo is firmly committed to promoting adoption of SofPulse® for all Hospital patient surgeries due to the significant reductions in post-operative pain. Recently, in a Baylor College of Medicine study in post-surgical pain and length of stay in Coronary artery bypass graft (CABG) cases, the SofPulse® study results demonstrated that the use of SofPulse® significantly decreased postoperative pain as measured by the VAS (Visual Analog Scale) by 50%, decreased opioid requirements (morphine equivalent dose) by 70%, and showed a significant decrease in the median Length of Stay (LOS) at the hospital by 2 days.” SofPulse®, through clinical and surgical studies, has shown significant pain reduction while providing a major cost savings when used for any surgery observed.It is suggested Widespread Hospital adaptation to SofPulse® as Standard of Care for post-operative surgical pain will require educating Hospitals and staff members. After understanding the significant cost savings and benefits that occur when SofPulse® is used as Standard of Care, we believe that they will begin to insist that SofPulse® is used for all in-patient surgeries.American Reporter reported in August 2020 that, “Adding SofPulse as Standard of Care for Coronary artery bypass graft (CBAG) cases yearly has a potential cost savings of over $5.7 billion dollars. Mr. Collier adds, “With over 500,000 of these types of open-heart types of surgeries alone, not including the numerous other types of surgeries with similar in-patient stays and recovery times, SofPulse® would offer Hospitals significant savings as well as be a revenue generator for increasing profits at those same Hospitals. The systemic benefits of expanding the use of SofPulse® technology in Orthopedic, Urology, and General surgery cases could far exceed the cost savings cited in the American Reporter article.”Mr. Collier continues, “SofPulse® device is FDA Cleared for reduction of pain and edema post-operatively. It offers a non-opioid, non-invasive, non-pharmaceutical opioid mitigation treatment and it has no known side effects based upon over 20,000+ surgical uses since its introduction to post-surgical pain management. Management believes that SofPulse® is a viable solution to manage pain and edema for all in-patient hospital surgeries. However, the true value of adopting this preventative approach to the opioid epidemic is in the lives saved. Imagine the number of lives impacted if patients required 70% less opioids to control their pain.”Mr. Collier concludes, “Endonovo's public awareness campaign will focus on educating Hospitals and MD's regarding SofPulse®’s proven ability to reduce pain and edema post-operatively while significantly reducing costs associated with surgeries. Through informing and educating the public and Medical professionals regarding opioid use and abuse prevention and the broadening usage of SofPulse®, an FDA cleared noninvasive Electroceutical® therapeutic device, we should be able to accomplish our goal of becoming standard of care for almost every surgery performed in the US.” About Endonovo TherapeuticsEndonovo Therapeutics, Inc. is a commercial-stage developer of noninvasive wearable Electroceuticals® therapeutic devices. The Company's current portfolio of commercial and clinical-stage wearable Electroceuticals® therapeutic devices addresses wound healing, pain, post-surgical pain and edema, cardiovascular disease, chronic kidney disease, and central nervous system (CNS) disorders, including traumatic brain injury (TBI), acute concussions, post-concussion syndrome and multiple sclerosis. The Company's noninvasive Electroceutical® therapeutic device, SofPulse®, which uses pulsed short-wave radiofrequency at 27.12 MHz, has been FDA-cleared and CE marked for the palliative treatment of soft tissue injuries and post-operative pain and edema and has CMS national coverage for the treatment of chronic wounds. The Company's current portfolio of preclinical-stage Electroceuticals® therapeutic devices addresses chronic kidney disease, liver disease, non-alcoholic steatohepatitis (NASH), cardiovascular and peripheral artery disease (PAD), and ischemic stroke. The Company's noninvasive, wearable Electroceuticals® therapeutic devices work by restoring key electrochemical processes that initiate anti-inflammatory and growth factor cascades necessary for healing to occur. www.endonovo.com.Safe Harbor StatementThis press release contains information that constitutes forward-looking statements made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. All statements, trends, analysis, and other information contained in this press release including words such as "anticipate," "believe," "plan," "estimate," "expect," "intend," and other similar expressions of opinion, constitute forward-looking statements. Any such forward-looking statements involve risks and uncertainties that could cause actual results to differ materially from any future results described within the forward-looking statements. Risk factors that could contribute to such differences include those matters more fully disclosed in the Company's reports filed with the Securities and Exchange Commission. The forward-looking information provided herein represents the Company's estimates as of the date of the press release, and subsequent events and developments may cause the Company's estimates to change. The Company specifically disclaims any obligation to update the forward-looking information in the future. Therefore, this forward-looking information should not be relied upon as representing the Company's estimates of its future financial performance as of any date subsequent to the date of this press release.Investor Relations Contact: Endonovo Therapeutics, Inc. Mr. Parker Mitchell (702) 742-8991 parker@regalconsultingllc.com www.endonovo.com1\. https://www.pharmacytimes.com/interviews/management-solutions-for-opioid-epidemic-are-similar-to-management-of-the-covid-19-pandemic 2\. https://www.drugabuse.gov/drug-topics/opioids/opioid-overdose-crisis 3\. https://www.theamericanreporter.com/endonovo-therapeutics-sofpulse-post-surgical-study-shows-decreased-post-operative-opioid-usage-and-decreased-length-of-stay-resulting-in-significant-cost-savings/

  • GlobeNewswire

    Endonovo Therapeutics Announces Encore Live Webinar of Baylor College of Medicine Study For Patients Undergoing Cardiothoracic Surgery Showing Reduction of Pain and Opioid Use With Significant Reduction of Length of Stay Using SofPulse®

    LOS ANGELES, Sept. 09, 2020 (GLOBE NEWSWIRE) -- Endonovo Therapeutics, Inc. (OTCQB: ENDV) ("Endonovo" or the "Company"), today announced an additional opportunity to view a live webinar presentation ‘The Impact of Pulsed Electromagnetic Field (SofPulse®) on Postoperative Pain in Patients Undergoing Cardiothoracic Surgery’ with Dr. Samir Awad, Professor of Surgery at Baylor College of Medicine on Thursday, September 17th at 5:00 pm Eastern Standard Time. The results of the study demonstrate that the use of SofPulse® significantly decreased postoperative pain VAS (Visual Analog Scale) by 50%, decreased postoperative opioid requirements (morphine equivalent dose) by 70% and resulted in a significant decrease in Length of Stay (LOS) at the hospital by a median of 2 days.The American Reporter article, published in August 2020, stated that “Coronary artery bypass graft (CABG) surgery is the most common type of open-heart surgery, and up to 500,000 CABG surgeries are performed in the US yearly with patient hospitalization averaging one week or 7 days.”The American Reporter article continued, “It is simply too hard to ignore the overall savings to hospitals if they simply added SofPulse® as a standard of care for all CABG cases yearly.” “A two-day reduction in the median Length of Stay (LOS) for CABG surgeries equates to a daily savings of $5,714, and a cumulative average realized savings to hospitals of $11,428 for each surgery performed.” “With 500,000 cases performed yearly in the US, the potential cost savings realized by hospitals could result in overall cost savings to in-patient and hospital care of $5,714,000,000.”Endonovo CEO Alan Collier states, “We are extremely honored to have the opportunity to support Dr. Awad in presenting these significant results utilizing the FDA Cleared SofPulse® PEMF device. The economic findings, cost savings and reduction of opioid use to hospitals and patients recovering from open heart type of surgeries from the Baylor College of Medicine study are stunning. Findings showing a significant reduction in the median Length of Stay (LOS) of 2 days for open heart type of surgeries proves that SofPulse® can provide hospitals significant savings on similar inpatient surgeries requiring postoperative pain management and opioid use.”Healthgrades.com, in August 2019 detailed, “The cost of CABG surgery varies greatly across the US with an average cost for CABG surgeries being $40,000.” Collier continued, “Study results demonstrate that simply using SofPulse® for postoperative pain and edema reduction offers hospitals a cost savings, from a reduction of the length of stay by 2 days, for patients to recover from these types of surgeries. With savings of $5,714 to $11,428 to hospitals per patient when using SofPulse® for these types of surgeries, we believe findings like these makes SofPulse® a viable option for reducing length of stay on any inpatient or outpatient surgical procedure done in the US.”The investigator initiated study, authored by Dr. Samir Awad, is entitled ‘The Impact of Pulsed Electromagnetic Field (SofPulse®) on Postoperative Pain in Patients Undergoing Cardiothoracic Surgery.’ The presentation was accepted for oral presentation at the 44th Annual meeting of the Association of VA Surgeons in 2020. The Study was conducted on 31 patients from 1/1/2019 thru 12/31/2019 with sixteen patients using SofPulse® adjunctively for recovery and fifteen patients not using SofPulse®. Both groups of patients were well matched with no significant difference in: Age, BMI, Gender, Comorbidities, ETOH, Tobacco or history of opioid use.The American Reporter article also noted in regard to the study, “Cost savings related to the reduction of opioid use and an overall improvement to the patient standard of care should be noted as well.”Dr. Awad will be presenting his research findings to his colleagues, the medical community and any interested parties in the general public.‘The Impact of Pulsed Electromagnetic Field (SofPulse®) on Postoperative Pain in Patients Undergoing Cardiothoracic Surgery’ webinar presentation is presently scheduled for Thursday, September 17th at 5pm EST.Please reserve your place today via email at webinar@endonovo.com.About Endonovo TherapeuticsEndonovo Therapeutics, Inc. is a commercial-stage developer of noninvasive wearable Electroceuticals® therapeutic devices. The Company's current portfolio of commercial and clinical-stage wearable Electroceuticals® therapeutic devices addresses wound healing, pain, post-surgical pain and edema, cardiovascular disease, chronic kidney disease, and central nervous system (CNS) disorders, including traumatic brain injury (TBI), acute concussions, post-concussion syndrome and multiple sclerosis. The Company's noninvasive Electroceutical® therapeutic device, SofPulse®, which uses pulsed short-wave radiofrequency at 27.12 MHz, has been FDA-cleared and CE marked for the palliative treatment of soft tissue injuries and post-operative pain and edema and has CMS national coverage for the treatment of chronic wounds. The Company's current portfolio of preclinical-stage Electroceuticals® therapeutic devices addresses chronic kidney disease, liver disease non-alcoholic steatohepatitis (NASH), cardiovascular and peripheral artery disease (PAD), and ischemic stroke. The Company's noninvasive, wearable Electroceuticals® therapeutic devices work by restoring key electrochemical processes that initiate anti-inflammatory and growth factor cascades necessary for healing to occur www.endonovo.com.Safe Harbor StatementThis press release contains information that constitutes forward-looking statements made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. All statements, trends, analysis, and other information contained in this press release including words such as "anticipate," "believe," "plan," "estimate," "expect," "intend," and other similar expressions of opinion, constitute forward-looking statements. Any such forward-looking statements involve risks and uncertainties that could cause actual results to differ materially from any future results described within the forward-looking statements. Risk factors that could contribute to such differences include those matters more fully disclosed in the Company's reports filed with the Securities and Exchange Commission. The forward-looking information provided herein represents the Company's estimates as of the date of the press release, and subsequent events and developments may cause the Company's estimates to change. The Company specifically disclaims any obligation to update the forward-looking information in the future. Therefore, this forward-looking information should not be relied upon as representing the Company's estimates of its future financial performance as of any date subsequent to the date of this press release.Investor Relations Contact:Endonovo Therapeutics, Inc. Mr. Parker Mitchell (702) 742-8991 parker@regalconsultingllc.comwww.endonovo.com

  • GlobeNewswire

    Endonovo Therapeutics, Inc. Announces Second Quarter Fiscal 2020 Financial Results

    LOS ANGELES, Aug. 20, 2020 (GLOBE NEWSWIRE) -- Endonovo Therapeutics, Inc. (OTCQB: ENDV) ("Endonovo" or the "Company"), today announced financial and operating results for the second quarter ended June 30, 2020.Key Financial Highlights:Operating Results for the Three Months Ended June 30, 2020 * Total Revenue was $44,631, a decrease of 28% compared to the same period last year * Gross Profit was $33,331, a 1% increase compared to the same period last year * Loss from Operations was $601,826, a 38% improvement compared to the same period last year * Net loss was $1.6 million, compared to a net loss of $7.8 million for the same period last year.Operating Results for the Six Months Ended June 30, 2020 * Total Revenue was $114,316, an increase of 6% compared to the same period last year * Gross Profit was $96,756, a 37% increase compared to the same period last year * Loss from Operations was $1.2 million, a 39% improvement compared to the same period last year * Net profit was $2.7 million, compared to a net loss of $10.2 million for the same period last year.Alan Collier, Endonovo’s Chief Executive Officer, stated, “The COVID-19 pandemic impacted our operations throughout the second quarter. Putting aside the impact of the pandemic, we did increase gross profit margins, which we believe demonstrates market acceptance of SofPulse® and illustrates our strategy implemented in 2019 has a unique opportunity for growth and market acceptance. Many of our customers, including hospitals, had suspended or were forced to limit certain medical procedures and operations due to the pandemic.”“As we enter the second half of the year, we are focused on expanding our sales channels and we continue to discuss and consider unique partnerships that can elevate SofPulse® as the leading medical device standard in post-operative care,” concluded Mr. Collier.About Endonovo TherapeuticsEndonovo Therapeutics, Inc. is a commercial-stage developer of non-invasive wearable Electroceuticals™ therapeutic devices. The Company's current portfolio of commercial and clinical-stage wearable Electroceuticals™ therapeutic devices addresses wound healing, pain, post-surgical pain and edema, cardiovascular disease, chronic kidney disease, and Central Nervous System (CNS) Disorders, including traumatic brain injury (TBI), acute concussions, post- concussion syndrome and multiple sclerosis. The Company's non-invasive Electroceutical™ therapeutic device, SofPulse®, using pulsed short-wave radiofrequency at 27.12 MHz has been FDA-Cleared and CE Marked for the palliative treatment of soft tissue injuries and post-operative pain and edema, and has CMS National Coverage for the treatment of chronic wounds. The Company's current portfolio of pre-clinical stage Electroceuticals™ therapeutic devices address chronic kidney disease, liver disease non-alcoholic steatohepatitis (NASH), cardiovascular and peripheral artery disease (PAD), and ischemic stroke. The Company's non-invasive, wearable Electroceuticals™ therapeutic devices work by restoring key electrochemical processes that initiate anti-inflammatory and growth factor cascades necessary for healing to occur. www.endonovo.com Safe Harbor StatementThis press release contains information that constitutes forward-looking statements made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. All statements, trends, analysis, and other information contained in this press release including words such as "anticipate," "believe," "plan," "estimate," "expect," "intend," and other similar expressions of opinion, constitute forward-looking statements. Any such forward-looking statements involve risks and uncertainties that could cause actual results to differ materially from any future results described within the forward-looking statements. Risk factors that could contribute to such differences include those matters more fully disclosed in the Company's reports filed with the Securities and Exchange Commission. The forward-looking information provided herein represents the Company's estimates as of the date of the press release, and subsequent events and developments may cause the Company's estimates to change. The Company specifically disclaims any obligation to update the forward-looking information in the future. Therefore, this forward-looking information should not be relied upon as representing the Company's estimates of its future financial performance as of any date subsequent to the date of this press release.Investor Relations Contact:Endonovo Therapeutics, Inc.Mr. Andrew Barwicki 516-662-9461 Andrew@barwicki.com www.endonovo.com