{"id":779641,"date":"2023-08-23T10:43:27","date_gmt":"2023-08-23T14:43:27","guid":{"rendered":"https:\/\/www.marketnewsdesk.com\/index.php\/abvc-biopharma-provides-updates-on-adhd-phase-iib-clinical-study\/"},"modified":"2023-08-23T10:43:27","modified_gmt":"2023-08-23T14:43:27","slug":"abvc-biopharma-provides-updates-on-adhd-phase-iib-clinical-study","status":"publish","type":"post","link":"https:\/\/www.marketnewsdesk.com\/index.php\/abvc-biopharma-provides-updates-on-adhd-phase-iib-clinical-study\/","title":{"rendered":"ABVC BioPharma Provides Updates on ADHD Phase IIb Clinical Study"},"content":{"rendered":"
\n

FREMONT, CA, Aug. 23, 2023 (GLOBE NEWSWIRE) — via NewMediaWire<\/a>\u00a0<\/b>\u2013\u00a0ABVC BioPharma, Inc<\/a>. (NASDAQ: ABVC) (“Company”), a clinical-stage biopharmaceutical company developing therapeutic solutions in oncology\/hematology, CNS, and ophthalmology, today announced that 60 subjects had been enrolled and 53 had completed the eight-week study for the Company’s ADHD Phase IIb clinical study. These subjects were enrolled at the University of California San Francisco (UCSF) Medical Center and five Taiwanese medical centers.<\/p>\n

The study entitled “A\u00a0Phase IIb Study of PDC-1421 Capsule to Evaluate the Safety and Efficacy in Patients with Adult Attention-Deficit\/Hyperactivity Disorder” is a randomized, double-blind, placebo-controlled study involving a total of approximately 100 patients in the United States and Taiwan. The Phase IIb clinical study continues the Phase IIa clinical study of ABV-1505. Phase IIa successfully achieved the specified primary endpoints at UCSF and was accepted by the U.S. Food & Drug Administration in October 2020.<\/p>\n

“At all of our sites, the enrollment of subjects participating in our ADHD Phase IIb study is going as planned,” said ABVC BioPharma Chief Executive Officer\u00a0Uttam Patil, Ph. D<\/a>. “To reach an interim analysis, the study requires 69 patients’ data. The remaining nine subjects are scheduled for screening in September. Our clinical trials continue to demonstrate that medicine derived from plants can have significant therapeutic benefits, often with few – if any – side effects when treating serious medical conditions.”<\/p>\n

According to the Polaris market research report, the global ADHD treatment market was valued at $16.13 billion in 2022 and is expected to reach $32.14 billion by 2030 with a CAGR of 7.1% over the forecast period.[1]<\/p>\n

About ABVC BioPharma<\/b>
ABVC BioPharma is a clinical-stage biopharmaceutical company with an active pipeline of six drugs and one medical device (ABV-1701\/Vitargus\u00ae) under development. For its drug products, the Company utilizes in-licensed technology from its network of world-renowned research institutions to conduct proof-of-concept trials through Phase II of clinical development. ABVC BioPharma’s network of research institutions includes Stanford University, the University of California at San Francisco, and Cedars-Sinai Medical Center. For Vitargus\u00ae, the Company intends to conduct global clinical trials through Phase III.<\/p>\n

Forward-Looking Statements<\/b>
This press release contains “forward-looking statements.” The words may precede such statements as “intends,” “may,” “will,” “plans,” “expects,” “anticipates,” “projects,” “predicts,” “estimates,” “aims,” “believes,” “hopes,” “potential,” or similar words. Forward-looking statements are not guarantees of future performance, are based on certain assumptions, and are subject to various known and unknown risks and uncertainties, many of which are beyond the Company’s control and cannot be predicted or quantified, and, consequently, actual results may differ materially from those expressed or implied by such forward-looking statements. Accordingly, none of the outcomes expressed herein are guaranteed. Such risks and uncertainties include, without limitation, risks and uncertainties associated with the following:<\/p>\n

    \n
  1. Our inability to manufacture our product candidates on a commercial scale on our own or in collaboration with third parties.<\/li>\n
  2. Difficulties in obtaining financing on commercially reasonable terms.<\/li>\n
  3. Changes in the size and nature of our competition.<\/li>\n
  4. Loss of one or more key executives or scientists.<\/li>\n
  5. Difficulties in securing regulatory approval to proceed to the next level of clinical trials or to market our product candidates.<\/li>\n<\/ol>\n

    More detailed information about the Company and the risk factors that may affect the realization of forward-looking statements is outlined in the Company’s filings with the Securities and Exchange Commission (SEC), including the Company’s Annual Report on Form 10-K and its Quarterly Reports on Form 10-Q. Investors are urged to read these documents free of charge on the SEC’s website at\u00a0http:\/\/www.sec.gov<\/a>. The Company assumes no obligation to publicly update or revise its forward-looking statements due to new information, future events, or otherwise.<\/p>\n

    \n
    Contact:
    Tom Masterson
    Email: tmasterson@allelecomms.com<\/p>\n

    [1]\u00a0https:\/\/www.prnewswire.com\/news-releases\/global-attention-deficit-hyperactivity-disorder-adhd-market-size-projected-to-reach-usd-32-14-billion-by-2032–with-cagr-of-7-1-study-by-polaris-market-research-301729196.html#:~:text=According%20to%20the%20research%20report,Deficit%20Hyperactivity%20Disorder%20(ADHD)%3F<\/a><\/p>\n


    \n
    \n \n <\/div>\n

    <\/div>\n","protected":false},"excerpt":{"rendered":"

    FREMONT, CA, Aug. 23, 2023 (GLOBE NEWSWIRE) — via NewMediaWire\u00a0\u2013\u00a0ABVC BioPharma, Inc. (NASDAQ: ABVC) (“Company”), a clinical-stage biopharmaceutical company developing therapeutic solutions in oncology\/hematology, CNS, and ophthalmology, today announced that 60 subjects had been enrolled and 53 had completed the eight-week study for the Company’s ADHD Phase IIb clinical study. These subjects were enrolled at the University of California San Francisco (UCSF) Medical Center and five Taiwanese medical centers. The study entitled “A\u00a0Phase IIb Study of PDC-1421 Capsule to Evaluate the Safety and Efficacy in Patients with Adult Attention-Deficit\/Hyperactivity Disorder” is a randomized, double-blind, placebo-controlled study involving a total of approximately 100 patients in the United States and Taiwan. The Phase IIb clinical study continues the Phase IIa clinical study … <\/p>\n

    Continue reading “ABVC BioPharma Provides Updates on ADHD Phase IIb Clinical Study”<\/span><\/a><\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[],"tags":[],"class_list":["post-779641","post","type-post","status-publish","format-standard","hentry"],"yoast_head":"\nABVC BioPharma Provides Updates on ADHD Phase IIb Clinical Study - Market Newsdesk<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.marketnewsdesk.com\/index.php\/abvc-biopharma-provides-updates-on-adhd-phase-iib-clinical-study\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"ABVC BioPharma Provides Updates on ADHD Phase IIb Clinical Study - Market Newsdesk\" \/>\n<meta property=\"og:description\" content=\"FREMONT, CA, Aug. 23, 2023 (GLOBE NEWSWIRE) — via NewMediaWire\u00a0\u2013\u00a0ABVC BioPharma, Inc. (NASDAQ: ABVC) (“Company”), a clinical-stage biopharmaceutical company developing therapeutic solutions in oncology\/hematology, CNS, and ophthalmology, today announced that 60 subjects had been enrolled and 53 had completed the eight-week study for the Company’s ADHD Phase IIb clinical study. These subjects were enrolled at the University of California San Francisco (UCSF) Medical Center and five Taiwanese medical centers. The study entitled “A\u00a0Phase IIb Study of PDC-1421 Capsule to Evaluate the Safety and Efficacy in Patients with Adult Attention-Deficit\/Hyperactivity Disorder” is a randomized, double-blind, placebo-controlled study involving a total of approximately 100 patients in the United States and Taiwan. 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