Aptevo Therapeutics Reports 3Q 2024 Financial Results and Provides a Business Update

ACCESSWIRE11-07

Company Achieves Milestones in Both Clinical Programs Initiates Mipletamig Phase 1b/2 Clinical Trial, "RAINIER," in Frontline Acute Myeloid Leukemia, Informed by Positive Dose Escalation Trial Results...

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}\n.meta {color:#5e5c6d;font-size:13px;margin:0 0 .5em; }\na{text-decoration:none; color:#2a4b87;}\n.meta .head { display: inline-block; overflow: hidden}\n.head .h-thumb { width: 30px; height: 30px; margin: 0; padding: 0; border-radius: 50%; float: left;}\n.head .h-content { margin: 0; padding: 0 0 0 9px; float: left;}\n.head .h-name {font-size: 13px; color: #eee; margin: 0;}\n.head .h-time {font-size: 11px; color: #7E829C; margin: 0;line-height: 11px;}\n.small {font-size: 12.5px; display: inline-block; transform: scale(0.9); -webkit-transform: scale(0.9); transform-origin: left; -webkit-transform-origin: left;}\n.smaller {font-size: 12.5px; display: inline-block; transform: scale(0.8); -webkit-transform: scale(0.8); transform-origin: left; -webkit-transform-origin: left;}\n.bt-text {font-size: 12px;margin: 1.5em 0 0 0}\n.bt-text p {margin: 0}\n</style>\n</head>\n<body>\n<div class=\"wrapper\">\n<header>\n<h2 class=\"title\">\nAptevo Therapeutics Reports 3Q 2024 Financial Results and Provides a Business Update\n</h2>\n\n<h4 class=\"meta\">\n\n\n2024-11-07 21:05 GMT+8&nbsp;&nbsp;&nbsp;<a href=https://finance.yahoo.com/news/aptevo-therapeutics-reports-3q-2024-130500926.html><strong>ACCESSWIRE</strong></a>\n\n\n</h4>\n\n</header>\n<article>\n<div>\n<p>Company Achieves Milestones in Both Clinical Programs\nInitiates Mipletamig Phase 1b/2 Clinical Trial, \"RAINIER,\" in Frontline Acute Myeloid Leukemia, Informed by Positive Dose Escalation Trial Results...</p>\n\n<a href=\"https://finance.yahoo.com/news/aptevo-therapeutics-reports-3q-2024-130500926.html\">Source Link</a>\n\n</div>\n\n\n</article>\n</div>\n</body>\n</html>\n","isBrief":false,"type":0,"news_type":1,"symbol":"SD","symbol_name":"SandRidge Energy","start_time":0,"source_url":"https://finance.yahoo.com/news/aptevo-therapeutics-reports-3q-2024-130500926.html","article_id":"2481902154","we_media_id":null,"thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2481902154","pubTimestamp":1730984700,"sourceInfo":{"source_id":"yahoofinance","name":"雅虎金融"},"weMediaInfo":null,"summary":"Initiates Mipletamig Phase 1b/2 Clinical Trial, \"RAINIER,\" in Frontline Acute Myeloid Leukemia, Informed by Positive Dose Escalation Trial Results. Presented Interim Data from ALG.APV-527 Phase 1 Trial in Multiple Solid Tumors at the European Society for Medical Oncology Congress. Additional Favorable Data to be Presented at the Society for Immunotherapy of Cancer Conference on November 8th. Based on positive safety, tolerability efficacy and durability data in its completed dose escalation trial, Aptevo Initiated the mipletamig Phase 1b/2 dose optimization trial, \"RAINIER,\" as part of its ongoing program to evaluate the compound in combination with standard of care venetoclax + azacitidine in frontline patients with acute myeloid leukemia . RAINIER will be conducted in two parts. First, a Phase 1b frontline AML dose optimization study followed by a Phase 2 study. \"Aptevo achieved significant clinical progress in both programs this quarter, marking important progress toward our mission","collect":0,"end_time":0,"defaultTopTitle":"yahoo.com","property":[],"viewcount":null,"language":"en","relate_stocks":{"SD":"SandRidge Energy","APVO":"Aptevo Therapeutics Inc.","BK4213":"石油与天然气的勘探与生产","BK4139":"生物科技"},"translate_title":"Aptevo Therapeutics报告2024年第三季度财务业绩并提供业务更新","themeId":null,"isJumpTheme":false,"ttsUrl":null,"symbols_score_info":{"APVO":1,"SD":1},"content_text":"Company Achieves Milestones in Both Clinical Programs\nInitiates Mipletamig Phase 1b/2 Clinical Trial, \"RAINIER,\" in Frontline Acute Myeloid Leukemia, Informed by Positive Dose Escalation Trial Results\nPresented Interim Data from ALG.APV-527 Phase 1 Trial in Multiple Solid Tumors at the European Society for Medical Oncology Congress\nAdditional Favorable Data to be Presented at the Society for Immunotherapy of Cancer Conference on November 8th\nRaises $5.75 Million in the Quarter\nSEATTLE, WA / ACCESSWIRE / November 7, 2024 / Aptevo Therapeutics Inc. (NASDAQ:APVO), a clinical-stage biotechnology company focused on developing novel immune-oncology therapeutics based on its proprietary ADAPTIR™ and ADAPTIR-FLEX™ platform technologies, today reported financial results for the quarter ending September 30, 2024 and provided a business update.\nBusiness HighlightsAptevo met multiple clinical milestones in the third quarter, including:\n\nBased on positive safety, tolerability efficacy and durability data in its completed dose escalation trial, Aptevo Initiated the mipletamig Phase 1b/2 dose optimization trial, \"RAINIER,\" as part of its ongoing program to evaluate the compound in combination with standard of care venetoclax + azacitidine in frontline patients with acute myeloid leukemia (AML). RAINIER will be conducted in two parts. First, a Phase 1b frontline AML dose optimization study followed by a Phase 2 study\nPresented positive interim data from their Phase 1 trial evaluating ALG.APV-527 as monotherapy for the treatment of solid tumors likely to express the tumor antigen 5T4 at the European Society of Medical Oncology (ESMO) Congress in September. Additional positive trial data will be presented at the Society for Immunotherapy of Cancer conference on November 8th.\nHighlights from the ESMO presentation include:\n\nClinical Activity/Efficacy: To date, nine of 15 efficacy evaluable patients (60%) have a best overall response of stable disease (SD). The longest SD duration was in a breast cancer patient who entered the study with progressive disease, achieved stable disease and remained on study for >11 months. This patient successfully transitioned to a higher dose level twice.\nSafety and Tolerability: ALG.APV-527 demonstrated a well-tolerated safety profile across all dose-level cohorts dosed to date.\nEvidence of biological activity: ALG.APV-527 could be measured in all patients with serum concentration of ALG.APV-527 consistent with the administered dose and preclinical predictions. Biomarker analyses confirm biological activity of ALG.APV-527\n\nClosed two financings for total proceeds of $5.75 million during the quarter\n\n\"Aptevo achieved significant clinical progress in both programs this quarter, marking important progress toward our mission and goals. We were thrilled to initiate the next phase of our mipletamig development program-a robust Phase 1b/2 trial for frontline AML patients, combining mipletamig with the established standard of care, venetoclax and azacitidine. This trial structure is informed by the encouraging results from our dose expansion trial, reinforcing our belief in mipletamig's transformative potential for AML patients,\" stated Marvin White, President and CEO of Aptevo. \"We also released positive interim data on our solid tumor drug, ALG.APV-527, at the European Society of Medical Oncology conference in September that further underscores the impact of our innovation. In early clinical evaluation, our solid tumor targeting bispecific demonstrated safety, tolerability, and compelling activity, with 60% of evaluable patients achieving stable disease in monotherapy across challenging tumor types, including breast and colon cancer. The progress we're witnessing, combined with nearly $6 million in capital secured in the quarter, sets a promising stage for the fourth quarter and lays the groundwork for continued successes into 2025.\"\n3Q Summary Financial Results\nCash Position: Aptevo had cash and cash equivalents totaling $7.8 million as of September 30, 2024.\nResearch and Development Expenses: Research and development expenses decreased by $0.8 million, from $3.9 million for the three months ended September 30, 2023, to $3.1 million for the three months ended September 30, 2024. The decrease was primarily due to lower spending on preclinical projects and employee costs.\nGeneral and Administrative Expenses: General and administrative expenses decreased by $0.6 million, from $2.7 million for the three months ended September 30, 2023, to $2.1 million for the three months ended September 30, 2024. The decrease is primarily due to lower employee and consulting costs.\nOther Income (Expense), Net:Other Income (Expense) from Continuing Operations, Net consists of other income, net of $0.1 million and $0.2 million for the three months ended September 30, 2024, and 2023, respectively. The change in other income, net is primarily due to the decrease of interest income from our money market accounts.\nNet Income (Loss): Aptevo had a net loss of $5.1 million or $0.48 per share for the three months ended September 30, 2024, compared to a net loss of $6.3 million or $22.16 per share for the corresponding period in 2023.\nAptevo Therapeutics Inc.CONDENSED CONSOLIDATED BALANCE SHEETS(in thousands, except share and per share amounts, unaudited)\n\n\n\n\n\n\n\n\n\nSeptember 30, 2024\n\n\nDecember 31, 2023\n\n\n\n\n\nASSETS\n\n\n\n\n\n\n\n\n\n\n\nCurrent assets:\n\n\n\n\n\n\n\n\n\n\n\nCash and cash equivalents\n\n\n$\n7,753\n\n\n$\n16,904\n\n\n\n\n\nPrepaid expenses\n\n\n\n1,635\n\n\n\n1,473\n\n\n\n\n\nOther current assets\n\n\n\n624\n\n\n\n689\n\n\n\n\n\nTotal current assets\n\n\n\n10,012\n\n\n\n19,066\n\n\n\n\n\nProperty and equipment, net\n\n\n\n614\n\n\n\n895\n\n\n\n\n\nOperating lease right-of-use asset\n\n\n\n4,520\n\n\n\n4,881\n\n\n\n\n\nTotal assets\n\n\n$\n15,146\n\n\n$\n24,842\n\n\n\n\n\nLIABILITIES AND STOCKHOLDERS' EQUITY\n\n\n\n\n\n\n\n\n\n\n\n\n\nCurrent liabilities:\n\n\n\n\n\n\n\n\n\n\n\n\n\nAccounts payable and other accrued liabilities\n\n\n$\n3,532\n\n\n$\n3,984\n\n\n\n\n\nAccrued compensation\n\n\n\n922\n\n\n\n2,098\n\n\n\n\n\nOther current liabilities\n\n\n\n1,428\n\n\n\n1,142\n\n\n\n\n\nTotal current liabilities\n\n\n\n5,882\n\n\n\n7,224\n\n\n\n\n\nOther long-term liabilities\n\n\n\n14\n\n\n\n-\n\n\n\n\n\nOperating lease liability\n\n\n\n4,830\n\n\n\n5,397\n\n\n\n\n\nTotal liabilities\n\n\n\n10,726\n\n\n\n12,621\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\nStockholders' equity:\n\n\n\n\n\n\n\n\n\n\n\n\n\nPreferred stock: $0.001 par value; 15,000,000 shares authorized, zero\n\n\nshares issued or outstanding\n\n\n\n-\n\n\n\n-\n\n\n\n\n\nCommon stock: $0.001 par value; 500,000,000 shares authorized;\n\n\n17,050,536 and 442,458 shares issued and outstanding at\n\n\nSeptember 30, 2024 and December 31, 2023, respectively\n\n\n\n82\n\n\n\n61\n\n\n\n\n\nAdditional paid-in capital\n\n\n\n245,603\n\n\n\n235,607\n\n\n\n\n\nAccumulated deficit\n\n\n\n(241,265\n)\n\n\n(223,447\n)\n\n\n\n\nTotal stockholders' equity\n\n\n\n4,420\n\n\n\n12,221\n\n\n\n\n\nTotal liabilities and stockholders' equity\n\n\n$\n15,146\n\n\n$\n24,842\n\n\n\n\n\n\nAptevo Therapeutics Inc.CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS(in thousands, except share and per share amounts, unaudited)\n\n\n\n\n\n\n\nFor the Three Months Ended September 30,\n\n\nFor the Nine Months Ended September 30,\n\n\n\n\n\n2024\n\n\n2023\n\n\n2024\n\n\n2023\n\n\n\n\n\nOperating expenses:\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\nResearch and development\n\n\n$\n(3,103\n)\n\n$\n(3,887\n)\n\n\n(10,498\n)\n\n\n(13,516\n)\n\n\n\n\nGeneral and administrative\n\n\n\n(2,110\n)\n\n\n(2,674\n)\n\n\n(7,722\n)\n\n\n(8,978\n)\n\n\n\n\nLoss from operations\n\n\n\n(5,213\n)\n\n\n(6,561\n)\n\n\n(18,220\n)\n\n\n(22,494\n)\n\n\n\n\nOther income:\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\nOther income from continuing operations, net\n\n\n\n112\n\n\n\n227\n\n\n\n402\n\n\n\n390\n\n\n\n\n\nGain related to sale of non-financial asset\n\n\n\n-\n\n\n\n-\n\n\n\n-\n\n\n\n9,650\n\n\n\n\n\nNet loss from continuing operations\n\n\n$\n(5,101\n)\n\n$\n(6,334\n)\n\n$\n(17,818\n)\n\n$\n(12,454\n)\n\n\n\n\nDiscontinued operations:\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\nIncome from discontinued operations\n\n\n$\n-\n\n\n$\n-\n\n\n$\n-\n\n\n$\n946\n\n\n\n\n\nNet loss\n\n\n$\n(5,101\n)\n\n$\n(6,334\n)\n\n$\n(17,818\n)\n\n$\n(11,508\n)\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\nBasic and diluted net loss per share from\n\n\ncontinuing operations:\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\nBasic\n\n\n$\n(0.48\n)\n\n$\n(22.16\n)\n\n$\n(5.01\n)\n\n$\n(60.84\n)\n\n\n\n\nDiluted\n\n\n$\n(0.48\n)\n\n$\n(22.16\n)\n\n$\n(5.01\n)\n\n$\n(60.84\n)\n\n\n\n\nBasic and diluted net loss per share:\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\nBasic\n\n\n$\n(0.48\n)\n\n$\n(22.16\n)\n\n$\n(5.01\n)\n\n$\n(56.22\n)\n\n\n\n\nDiluted\n\n\n$\n(0.48\n)\n\n$\n(22.16\n)\n\n$\n(5.01\n)\n\n$\n(56.22\n)\n\n\n\n\nShares used in calculation:\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\nBasic\n\n\n\n10,548,470\n\n\n\n285,886\n\n\n\n3,554,796\n\n\n\n204,694\n\n\n\n\n\nDiluted\n\n\n\n10,548,470\n\n\n\n285,886\n\n\n\n3,554,796\n\n\n\n204,694\n\n\n\n\n\n\nAbout Aptevo Therapeutics Inc.Aptevo Therapeutics Inc. is a clinical-stage biotechnology company focused on developing novel immuno-oncology therapies for the treatment of cancer. Aptevo is seeking to improve treatment outcomes for cancer patients. For more information, please visit www.aptevotherapeutics.com.\nSafe Harbor StatementThis press release includes forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. All statements, other than statements of historical fact, including, without limitation, Aptevo's expectations about the activity, efficacy, safety, tolerability and durability of its therapeutic candidates and potential use of any such candidates, including in combination with other drugs, as therapeutics for treatment of disease, its expectations regarding the effectiveness of its ADAPTIR and ADAPTIR-FLEX platforms, statements related to the progress of Aptevo's clinical programs, including statements related to anticipated clinical and regulatory milestones, whether further study of mipletamig in a Phase 1b dose optimization trial focusing on multiple doses of mipletamig in combination with venetoclax + azacitidine on a targeted patient population will continue to show clinical benefit, whether Aptevo's final trial results will vary from its earlier assessment, whether further study of ALG.APV-527 across multiple tumor types will continue to show clinical benefit, whether higher dose ranges for ALG.APV-527 will result in increased signs of clinical activity, whether biomarker analyses will continue to confirm biological activity of ALG.APV-527, the possibility and timing of future preliminary or interim data readouts for ALG.APV-527, whether Aptevo's final trial results will vary from its preliminary or interim assessments, statements related to the progress of and enthusiasm for Aptevo's clinical programs, statements related to Aptevo's cash position and balance sheet, statements related to Aptevo's ability to generate stockholder value, whether Aptevo will continue to have momentum in its business in the future, and any other statements containing the words \"may,\" \"continue to,\" \"believes,\" \"knows,\" \"expects,\" \"optimism,\" \"potential,\" \"designed,\" \"promising,\" \"plans,\" \"will\" and similar expressions are intended to identify forward-looking statements. These forward-looking statements are based on Aptevo's current intentions, beliefs, and expectations regarding future events. Aptevo cannot guarantee that any forward-looking statement will be accurate. Investors should realize that if underlying assumptions prove inaccurate or unknown risks or uncertainties materialize, actual results could differ materially from Aptevo's expectations. Investors are, therefore, cautioned not to place undue reliance on any forward-looking statement.\nThere are several important factors that could cause Aptevo's actual results to differ materially from those indicated by such forward-looking statements, including a deterioration in Aptevo's business or prospects; further assessment of preliminary or interim data or different results from later clinical trials; adverse events and unanticipated problems, adverse developments in clinical development, including unexpected safety issues observed during a clinical trial; and changes in regulatory, social, macroeconomic and political conditions. For instance, actual results may differ materially from those indicated by such forward-looking statements as a result of various important factors, including the uncertainties inherent in the results of preliminary or interim data and preclinical studies being predictive of the results of later-stage clinical trials, initiation, enrollment and maintenance of patients, and the completion of clinical trials, the availability and timing of data from ongoing clinical trials, the trial design includes combination therapies that may make it difficult to accurately ascertain the benefits of mipletamig, expectations for the timing and steps required in the regulatory review process, expectations for regulatory approvals, the impact of competitive products, our ability to enter into agreements with strategic partners or raise funds on acceptable terms or at all and other matters that could affect the availability or commercial potential of Aptevo's product candidates, business or economic disruptions due to catastrophes or other events, including natural disasters or public health crises such as the coronavirus (referred to as COVID-19), geopolitical risks, including the current war between Russia and Ukraine, war between Israel and Hamas, and macroeconomic conditions such as economic uncertainty, rising inflation and interest rates, continued market volatility and decreased consumer confidence and uncertainty in the impact of the results of the United States presidential election and congressional election. These risks are not exhaustive, Aptevo faces known and unknown risks. Additional risks and factors that may affect results are set forth in Aptevo's filings with the Securities and Exchange Commission, including its Annual Report on Form 10-K for the fiscal year ended December 31, 2023, and its subsequent reports on Form 10-Q and current reports on Form 8-K. The foregoing sets forth many, but not all, of the factors that could cause actual results to differ from Aptevo's expectations in any forward-looking statement. Any forward-looking statement speaks only as of the date of this press release, and, except as required by law, Aptevo does not assume any obligation to update any forward-looking statement to reflect new information, events, or circumstances.\nCONTACT:Miriam Weber MillerHead, Investor Relations & Corporate CommunicationsAptevo TherapeuticsEmail: IR@apvo.com or Millerm@apvo.comPhone: 206-859-6628\nSOURCE: Aptevo Therapeutics\n\nView the original \npress release on accesswire.com","kind":null,"is_publish_news":true,"is_publish_highlight":false,"is_publish_live":false,"is_publish_wemedia":null,"editions":null,"column":"","sentiment":"0","news_tag":"","news_rank":0,"symbols":[],"gpt_button":1},"commentList":[],"isCommentEnd":true,"newsSizeData":{"likeSize":0,"commentSize":0,"repostSize":0,"favoriteSize":0,"likeStatus":false,"favoriteStatus":false},"APP":{"userAgent":"Mozilla/5.0 AppleWebKit/537.36 (KHTML, like Gecko; compatible; ClaudeBot/1.0; +claudebot@anthropic.com)","isDev":false,"isTTM":true,"deviceId":"web-server-community-laohu8-v3","version":"4.29.1","shortVersion":"4.29.1","platform":"web","vendor":"web","appName":"ttm","isIOS":false,"isAndroid":false,"isTiger":false,"isTHS":false,"isWeiXin":false,"isWeiXinMini":false,"isWeiBo":false,"isQQ":false,"isBaiduSwan":false,"isBaiduBox":false,"isDingTalk":false,"isToutiao":false,"isOnePlus":false,"isHuaWei":false,"isXiaomi":false,"isXiaomiWebView":false,"isOppo":false,"isVivo":false,"isSamsung":false,"isMobile":false},"href":"/m/news/2481902154"}