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Oncology Pharma Year End Review and Outlook

Oncology Pharma Year End Review and Outlook

腫瘤製藥年終回顧與展望
Accesswire ·  2021/12/09 21:37

SAN FRANCISCO, CA / ACCESSWIRE / December 9, 2021 / Oncology Pharma Inc. (OTC PINK:ONPH) - Oncology Pharma, Inc. ("The Company") and its Chief Executive are pleased to give a year end update and provide an outlook for what to look for in the coming months and year ahead. The Company is proud of the progress it has made this past year including the addition of a renowned Chairman to the Scientific Advisory Board, retaining a PCAOB audit firm, commencing financing and work on drug research and studies with a highly experienced team as further described below. The Company has further signed additional licensing agreements throughout the year that it believes will enhance the growth of the Company. It looks forward to continuing, expanding and accelerating the work in the coming year.

加利福尼亞州舊金山/ACCESSWIRE/2021年12月9日/Oncology Pharma Inc.(場外交易PINK: ONPH)——Oncology Pharma, Inc.(“公司”)及其首席執行官很高興提供年終最新情況,並對未來幾個月和未來一年的展望。公司爲去年取得的進展感到自豪,包括增加了一位著名的科學顧問委員會主席,保留了一家PCAOB審計公司,開始融資並與一支經驗豐富的團隊一起進行藥物研究和研究,詳情見下文。該公司全年進一步簽署了其他許可協議,它認爲這些協議將促進公司的發展。它期待着在來年繼續、擴大和加快這項工作。

Oncology Pharma, Inc. is a pioneering oncology company dedicated to providing the financing and the tools to license, develop, manufacture, and commercialize therapeutics. Over the past several years the Company has assembled a team of executives and advisors with proven multi-disciplinary expertise in the fields of oncology and therapeutics with leadership to identify, negotiate and amalgamate "best in class" research, technologies, therapeutics and delivery mechanisms that are synergistic and collaborative. As stated before, the Company's goal is to create value, reduce costs and increase the speed of regulatory approval and commercialization of effective and safer cancer drugs.

Oncology Pharma, Inc. 是一家開創性的腫瘤學公司,致力於爲療法的許可、開發、製造和商業化提供融資和工具。在過去的幾年中,公司組建了一支由在腫瘤學和治療學領域具有成熟的多學科專業知識的高管和顧問組成的團隊,負責確定、談判和整合 “一流的” 研究、技術、療法和具有協同作用的交付機制。如前所述,該公司的目標是創造價值,降低成本並提高有效和更安全的抗癌藥物的監管批准和商業化的速度。

Oncology Pharma's strategy centers on progressing its licensed products through initial phases of development and finding the appropriate path to commercial success and value creation for its stakeholders. The Company has specifically chosen during these initial phases to focus on pediatrics and the potential orphan drug designation, for which the Company is currently working towards submitting its first application. The capital outlay is projected to be significantly lower than traditional drug development programs and there is a high need for improved therapies for patients with rare cancers with the potential for Oncology Pharma to positively impact these patients worldwide. It is the Company's position that what it is pursuing is groundbreaking and that the pediatric market has been underserved by big pharma, which may allow for significant developments in this field and give the potential for the Company to stand out amongst its peers.

Oncology Pharma的戰略重點是在許可產品開發的初始階段取得進展,併爲其利益相關者找到實現商業成功和創造價值的適當途徑。在這些初始階段,該公司特別選擇將重點放在兒科和潛在的孤兒藥指定上,該公司目前正在努力提交第一份申請。預計資本支出將大大低於傳統藥物開發計劃,對於罕見癌症患者,急需改進療法,Oncology Pharma有可能在全球範圍內對這些患者產生積極影響。該公司的立場是,其追求的是開創性的,大型製藥公司對兒科市場的服務不足,這可能允許該領域取得重大發展,並使公司有可能在同行中脫穎而出。

As stated in Oncology Pharma's previous press release, the initial drug product being developed is a nanoemulsion of dactinomycin. Dactinomycin was approved by the FDA more than 50 years ago but has been limited in its utility due to severe toxic side-effects at effective doses. The Company believes the novel formulation currently in development can overcome this limitation by creating a safer and potentially more effective drug formulation. This formulation may also enable greater accumulation of the drug at the tumor site, potentially increasing its tumor-kill effectiveness while simultaneously sparing healthy tissues.

正如Oncology Pharma先前的新聞稿中所述,正在開發的初始藥物產品是放射黴素的納米乳液。50多年前,Dactinomycin獲得了FDA的批准,但由於有效劑量下會產生嚴重的毒性副作用,其效用受到限制。該公司認爲,目前正在開發的新配方可以通過創造一種更安全、可能更有效的藥物配方來克服這一限制。這種配方還可以增加藥物在腫瘤部位的積累,有可能提高其殺滅腫瘤的有效性,同時保護健康組織。

Studies and research have commenced. Initial feasibility work for this proprietary nanoemulsion of dactinomycin is currently underway. It is the Company's belief that this delivery will have broad and far-ranging applications beyond oncology. The goal is to move this process into the clinical studies phase as our current research and studies will permit.

研究和研究已經開始。這種專有的 dactinomycin 納米乳液的初步可行性研究目前正在進行中。該公司相信,這種交付將在腫瘤學之外具有廣泛而廣泛的應用。目標是在我們目前的研究允許的情況下,將這一過程推進到臨床研究階段。

Oncology Pharma is also in the midst of finalizing all necessary steps to complete its audit after it has retained its PCAOB qualified auditors as disclosed in the press release on October 12, 2021. The Company expects this process to be completed in the coming weeks. If successful, this would make progress towards the goal of being able to complete an application to uplist to the Capital Markets Tier of NASDAQ.

正如2021年10月12日的新聞稿所披露的那樣,Oncology Pharma在保留了PCAOB合格的核數師後,也正在敲定所有必要步驟以完成審計。該公司預計這一過程將在未來幾周內完成。如果成功,這將朝着能夠完成納斯達克資本市場層上行申請的目標取得進展。

During this past year Oncology Pharma has also signed license agreements with Regen BioPharma, Inc. for its small molecule and for the mRNA technology to address colon cancer and pancreatic cancer. It is the Company's intent that in the beginning of next year it will further engage with our team to advance these licenses along the same path as we have with the nanoemulsion of dactinomycin.

在過去的一年中,Oncology Pharma還與Regen BioPharma, Inc.簽署了許可協議,涉及其小分子以及用於治療結腸癌和胰腺癌的mRNA技術。該公司打算在明年年初進一步與我們的團隊合作,沿着與發放黴素納米乳液相同的道路推進這些許可。

The Company is also in the midst of advancing its commitment to Ribeira Solutions' Connect2Med patient engagement platform and retention technology. Connect2Med provides a motivating trial experience through increased engagement and easy to use communication tools. They have access to a dedicated trial specific portal (patient facing app), where they can perform functions like eDiary, ePRO and telehealth visits. The platform is FHIR compatible and easily integrates with EHR, CTMS, CRM from major vendors in the industry. Patients' workflow can be automated through a set of digital workflows, with automated interventions and escalation when needed. Sites and CROs can post upcoming trials in a public space for all to see, boosting public awareness through social sharing. Site owners and Sponsors have access to impactful data, metrics and reports that allow them to make strategic decisions to improve retention, growth, performance, satisfaction and ROI.

該公司還在推進其對Ribeira Solutions的Connect2Med患者參與平台和留存技術的承諾。Connect2Med 通過增加參與度和易於使用的溝通工具,提供激勵人心的試驗體驗。他們可以訪問專門的試驗門戶(面向患者的應用程序),在那裏他們可以執行eDiary、ePro和遠程醫療就診等功能。該平台兼容 FHIR,可輕鬆與業內主要供應商的 EHR、CTMS、CRM 集成。患者的工作流程可以通過一組數字工作流程實現自動化,並在需要時進行自動干預和升級。網站和CRO可以在公共場所發佈即將進行的試驗以供所有人觀看,通過社交分享提高公衆意識。網站所有者和贊助商可以訪問有影響力的數據、指標和報告,使他們能夠做出戰略決策,以提高留存率、增長、績效、滿意度和投資回報率。

Oncology Pharma has been able to pursue multiple avenues and maintain focus throughout 2021. The Company expects to continue this work and pursue developments through its engaged relationships and license agreements, while seeking value for its stakeholders. Additional information will be provided as it becomes available.

在整個2021年,Oncology Pharma已經能夠尋求多種途徑並保持專注。該公司希望繼續開展這項工作,通過其合作關係和許可協議尋求發展,同時爲利益相關者尋求價值。其他信息將在可用時提供。

ABOUT ONCOLOGY PHARMA, INC.

關於腫瘤製藥公司

ONCOLOGY PHARMA, INC. (OTC PINK:ONPH) (the 'Company') is currently engaging in research and development of therapeutics for oncology and prides itself for having a world-class Advisory Board that keeps the Company in the forefront of developing technologies in cancer research, biotechnology, and healthcare.

腫瘤製藥公司(OTC PINK: ONPH)(“公司”)目前正在研究和開發腫瘤療法,並以擁有世界一流的顧問委員會而自豪,該委員會使公司處於癌症研究、生物技術和醫療保健技術開發的最前沿。

FORWARD LOOKING STATEMENTS

前瞻性陳述

Certain of the matters discussed in this announcement contain forward-looking statements that involve material risks to and uncertainties in the Company's business that may cause actual results to differ materially from those anticipated by the statements made herein. Such risks and uncertainties include risks related to licensing arrangements and joint ventures, including the need to negotiate the definitive agreements for the relationships; possible failure to realize anticipated benefits of business relationships, and costs of providing funding to these business relationships. Other risks and uncertainties relating to the Company include, among other things, current negative operating cash flows and a need for additional funding to finance our operating plan; the terms of any further financing, which may be highly dilutive and may include onerous terms; unexpected costs and operating deficits, and lower than expected sales and revenues; uncertain willingness and ability of customers to adopt new technologies and other factors that may affect further market acceptance; adverse economic conditions; adverse results of any legal proceedings; the volatility of our operating results and financial condition; inability to attract or retain qualified senior management personnel, including sales and marketing personnel; our ability to establish and maintain the proprietary nature of our technology through the patent process, as well as our ability to possibly license from others patents and patent applications necessary to develop products; the Company's ability to implement its long range business plan for various applications of its technology; the Company's ability to enter into agreements with any necessary marketing and/or distribution partners and with any strategic or joint venture partners; the impact of competition; the obtaining and maintenance of any necessary regulatory clearances applicable to applications of the Company's technology; management of growth; and, other risks and uncertainties. This is not a solicitation to buy or sell securities and does not purport to be an analysis of the Company's financial position.

本公告中討論的某些事項包含前瞻性陳述,涉及公司業務的重大風險和不確定性,可能導致實際業績與本文陳述的預期存在重大差異。此類風險和不確定性包括與許可安排和合資企業有關的風險,包括需要就關係談判最終協議;可能無法實現業務關係的預期收益,以及爲這些業務關係提供資金的成本。與公司相關的其他風險和不確定性包括當前運營現金流爲負以及需要額外資金來爲我們的運營計劃提供資金;任何進一步融資的條款,可能具有高度稀釋性,可能包括繁瑣的條款;意外的成本和運營赤字以及低於預期的銷售和收入;客戶採用新技術的意願和能力以及可能影響進一步市場接受度的其他因素;不利的經濟狀況;任何法律訴訟的不利結果;我們經營業績和財務狀況的波動性;無法吸引或留住合格的高級管理人員,包括銷售和營銷人員;我們通過專利程序建立和維護我們技術的專有性質的能力,以及我們可能從開發產品所需的其他專利和專利申請中獲得許可的能力;公司實施其技術各種應用的長期業務計劃的能力;公司與任何人簽訂協議的能力必要的營銷和/或分銷合作伙伴以及與任何戰略或合資夥伴的關係;競爭的影響;獲得和維持適用於公司技術應用的任何必要監管許可;增長管理;以及其他風險和不確定性。這不是買入或賣出證券的邀請,也無意對公司財務狀況的分析。

CONTACTS:

聯繫人:

For additional information, please contact the Oncology Pharma at:

欲了解更多信息,請通過以下方式聯繫腫瘤製藥公司:

One Sansome Street, Suite 3500
San Francisco, CA 94104
Phone: 415-869-1038
Fax: 415-946-8801
website: www.oncology-pharma.com
email: info@oncology-pharma.com

桑索姆街一號,3500 套房
加利福尼亞州舊金山 94104
電話:415-869-1038
傳真:415-946-8801
網站:www.oncology-pharma.com
電子郵件:info@oncology-pharma.com

SOURCE: Oncology Pharma Inc.

來源:腫瘤學制藥公司


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