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Panbela to Host Third Quarter 2024 Earnings Conference Call on November 14, 2024

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Panbela Therapeutics (OTCQB: PBLA), a clinical stage company focused on developing treatments for urgent unmet medical needs, has scheduled its Q3 2024 earnings conference call for November 14, 2024, at 4:30 PM Eastern Time. The call will discuss financial results for the quarter ended September 30, 2024. The company has provided both domestic and international dial-in numbers, along with webcast access for interested participants.

Panbela Therapeutics (OTCQB: PBLA), una compagnia in fase clinica focalizzata sullo sviluppo di trattamenti per bisogni medici urgenti non soddisfatti, ha programmato la sua conference call sugli utili del Q3 2024 per il 14 novembre 2024, alle 16:30 ora orientale. La call discuterà i risultati finanziari per il trimestre conclusosi il 30 settembre 2024. L'azienda ha fornito numeri di accesso sia nazionali che internazionali, insieme a un link per il webcast per i partecipanti interessati.

Panbela Therapeutics (OTCQB: PBLA), una empresa en etapa clínica enfocada en desarrollar tratamientos para necesidades médicas urgentes no satisfechas, ha programado su llamada de conferencia sobre ganancias del Q3 2024 para el 14 de noviembre de 2024, a las 16:30 hora oriental. La llamada discutirá los resultados financieros para el trimestre que terminó el 30 de septiembre de 2024. La empresa ha proporcionado números de acceso tanto nacionales como internacionales, junto con acceso a la transmisión en vivo para los participantes interesados.

판벨라 테라퓨틱스 (OTCQB: PBLA), 긴급한 의료 요구를 충족하는 치료제를 개발하는 데 중점을 둔 임상 단계 회사가 2024년 3분기 실적 컨퍼런스 콜을 2024년 11월 14일 오후 4시 30분(동부 표준시)으로 예정했습니다. 이 통화에서는 2024년 9월 30일 종료된 분기의 재무 결과에 대해 논의할 것입니다. 회사는 관심 있는 참가자를 위해 국내외 접속 번호와 웹캐스트 액세스를 제공했습니다.

Panbela Therapeutics (OTCQB: PBLA), une entreprise en phase clinique axée sur le développement de traitements pour des besoins médicaux urgents non satisfaits, a prévu sa conférence téléphonique sur les résultats du 3ème trimestre 2024 pour le 14 novembre 2024 à 16h30, heure de l'Est. La conférence discutera des résultats financiers pour le trimestre clos le 30 septembre 2024. L'entreprise a fourni des numéros d'appel nationaux et internationaux, ainsi qu'un accès à la diffusion en direct pour les participants intéressés.

Panbela Therapeutics (OTCQB: PBLA), ein Unternehmen in der klinischen Phase, das sich auf die Entwicklung von Behandlungen für dringend benötigte medizinische Bedürfnisse konzentriert, hat seine Q3 2024 Ergebniskonferenzschaltung für den 14. November 2024 um 16:30 Uhr Eastern Time angesetzt. Die Konferenz wird die finanziellen Ergebnisse für das Quartal, das am 30. September 2024 endete, besprechen. Das Unternehmen hat sowohl nationale als auch internationale Einwahlnummern sowie Zugang zur Webcast-Übertragung für interessierte Teilnehmer bereitgestellt.

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MINNEAPOLIS, Oct. 31, 2024 (GLOBE NEWSWIRE) -- Panbela Therapeutics, Inc. (OTCQB: PBLA), (“Panbela”), a clinical stage company developing disruptive therapeutics for the treatment of patients with urgent unmet medical needs, today announced that it will host a conference call on November 14, 2024, at 4:30 PM Eastern Time to discuss results for its third quarter ended September 30, 2024.

Conference Call Information
Toll Free: 877-545-0320
International: 973-528-0002
Participant Access Code: 370494
Webcast Link: https://www.webcaster4.com/Webcast/Page/2556/51548

Conference Call Replay Information
Toll Free: 877-481-4010
International: 919-882-2331
Replay Passcode: 51548
Webcast Replay: https://www.webcaster4.com/Webcast/Page/2556/51548

About Panbela’s Pipeline
The pipeline consists of assets currently in clinical trials with an initial focus on familial adenomatous polyposis (FAP), first-line metastatic pancreatic cancer, neoadjuvant pancreatic cancer, colorectal cancer prevention and ovarian cancer. The combined development programs have a steady cadence of anticipated catalysts with programs ranging from pre-clinical to registration studies.

Ivospemin (SBP-101)
Ivospemin is a proprietary polyamine analogue designed to induce polyamine metabolic inhibition (PMI) by exploiting an observed high affinity of the compound for pancreatic ductal adenocarcinoma and other tumors. It has shown signals of tumor growth inhibition in clinical studies of metastatic pancreatic cancer patients, demonstrating a median overall survival (OS) of 14.6 months and an objective response rate (ORR) of 48%, both exceeding what is typical for the standard of care of gemcitabine + nab-paclitaxel suggesting potential complementary activity with the existing FDA-approved standard chemotherapy regimen. In data evaluated from clinical studies to date, ivospemin has not shown exacerbation of bone marrow suppression and peripheral neuropathy, which can be chemotherapy-related adverse events. Serious visual adverse events have been evaluated and patients with a history of retinopathy or at risk of retinal detachment will be excluded from future SBP-101 studies. The safety data and PMI profile observed in the previous Panbela-sponsored clinical trials provide support for continued evaluation of ivospemin in the ASPIRE trial.

Flynpovi ™
Flynpovi is a combination of CPP-1X (eflornithine) and sulindac with a dual mechanism inhibiting polyamine synthesis and increasing polyamine export and catabolism. In a Phase III clinical trial in patients with sporadic large bowel polyps, the combination prevented > 90% subsequent pre-cancerous sporadic adenomas versus placebo. Focusing on FAP patients with lower gastrointestinal tract anatomy in the recent Phase III trial comparing Flynpovi to single agent eflornithine and single agent sulindac, FAP patients with lower GI anatomy (patients with an intact colon, retained rectum or surgical pouch), showed statistically significant benefit compared to both single agents (p≤0.02) in delaying surgical events in the lower GI for up to four years. The safety profile for Flynpovi did not significantly differ from the single agents and supports the continued evaluation of Flynpovi for FAP.

CPP-1X
CPP-1X (eflornithine) is being developed as a single agent tablet or high dose powder sachet for several indications including prevention of gastric cancer, treatment of neuroblastoma and recent onset Type 1 diabetes. Preclinical studies as well as Phase I or Phase II investigator-initiated trials suggest that CPP-1X treatment may be well-tolerated and has potential activity.

About Panbela
Panbela Therapeutics, Inc. is a clinical-stage biopharmaceutical company developing disruptive therapeutics for patients with urgent unmet medical needs. Panbela’s lead assets are Ivospemin (SBP-101) and Flynpovi. Further information can be found at www.panbela.com. Panbela’s common stock is eligible for quotation on the OTCQB under the symbol “PBLA”.

Cautionary Statement Regarding Forward-Looking Statements
This press release contains “forward-looking statements,” including within the meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking statements can be identified by words such as: “anticipate,” “believe,” “can,” “design,” “expect,” “focus,” “intend,” “looking forward,” “may,” “plan,” “positioned,” “potential,” and “will.” All statements other than statements of historical fact are statements that should be deemed forward-looking statements. Forward-looking statements are neither historical facts nor assurances of future performance. Instead, they are based only on our current beliefs, expectations, and assumptions regarding the future of our business, future plans and strategies, projections, anticipated events and trends, the economy and other future conditions. Because forward-looking statements relate to the future, they are subject to inherent uncertainties, risks and changes in circumstances that are difficult to predict and many of which are outside of our control. Our actual results and financial condition may differ materially and adversely from the forward-looking statements. Therefore, you should not rely on any of these forward-looking statements. Important factors that could cause our actual results and financial condition to differ materially from those indicated in the forward-looking statements include, among others, the following: (i) our ability to obtain additional capital, on acceptable terms or at all, required to implement our business plan; (ii) our lack of diversification and the corresponding risk of an investment in our Company and the corresponding risk of potential deterioration of our financial condition and results due to failure to diversify; (iii) our ability to obtain and maintain our listing on a national securities exchange; (iv) results, progress and success of our randomized Phase Ia/Ib and Phase II/III clinical trials; (v) our ability to demonstrate the safety and effectiveness of our product candidates: ivospemin ( SBP-101 ), Flynpovi, and eflornithine (CPP-1X); (vi) potential delays or risks to the success of our randomized Phase II/III clinical trial resulting from a termination in our relationship with our CRO; (vii) our ability to obtain regulatory approvals for our product candidates, SBP-101, Flynpovi and CPP-1X in the United States, the European Union or other international markets; (viii) the market acceptance and level of future sales of our product candidates, SBP-101, Flynpovi and CPP-1X ; (ix) the cost and delays in product development that may result from changes in regulatory oversight applicable to our product candidates, SBP-101, Flynpovi and CPP-1X ; (x) the rate of progress in establishing reimbursement arrangements with third-party payors; (xi) the effect of competing technological and market developments; (xii) the costs involved in filing and prosecuting patent applications and enforcing or defending patent claims; and (xiii) such other factors as discussed in Part I, Item 1A under the caption “Risk Factors” in our most recent Annual Report on Form 10-K , any additional risks presented in our Quarterly Reports on Form 10-Q and our Current Reports on Form 8-K. Any forward-looking statement made by us in this press release is based on information currently available to us and speaks only as of the date on which it is made. We undertake no obligation to publicly update any forward-looking statement or reasons why actual results would differ from those anticipated in any such forward-looking statement, whether written or oral, whether as a result of new information, future developments or otherwise.

Contact Information:

Investors:
James Carbonara
Hayden IR
(646) 755-7412
james@haydenir.com

Media:
Tammy Groene
Panbela Therapeutics, Inc.
(952) 479-1196
IR@panbela.com


FAQ

When is Panbela Therapeutics (PBLA) Q3 2024 earnings call?

Panbela Therapeutics (PBLA) will host its Q3 2024 earnings conference call on November 14, 2024, at 4:30 PM Eastern Time.

How can I access Panbela Therapeutics (PBLA) Q3 2024 earnings call?

You can access the call via toll-free number 877-545-0320 (US) or 973-528-0002 (International) using participant code 370494. A webcast is also available through the company's investor portal.

What period will Panbela Therapeutics (PBLA) Q3 2024 earnings cover?

The earnings call will cover Panbela Therapeutics' third quarter results for the period ended September 30, 2024.

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