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[8-K] Phibro Animal Health Corporation Reports Material Event

Filing Impact
(Neutral)
Filing Sentiment
(Neutral)
Form Type
8-K
Rhea-AI Filing Summary

Aclaris Therapeutics (Nasdaq: ACRS) has filed a Form 8-K to inform investors that it will host a conference call on 29 Jul 2025 to review top-line data from its Phase 2a study of ATI-2138, an oral covalent ITK/JAK3 inhibitor for moderate-to-severe atopic dermatitis. Two items are furnished: Exhibit 99.1 (investor presentation) and Exhibit 99.2 (press release). Under Reg FD, Items 7.01 and 8.01 are furnished—not filed—so the information is not subject to Exchange Act liability nor automatically incorporated into other SEC reports.

The 8-K contains no numerical efficacy, safety, or financial metrics. Investors must consult the accompanying exhibits or join the conference call for detailed results. No changes to financial statements or previously issued guidance are included.

Aclaris Therapeutics (Nasdaq: ACRS) ha presentato un modulo 8-K per informare gli investitori che terrà una conference call il 29 luglio 2025 per esaminare i dati preliminari del suo studio di Fase 2a su ATI-2138, un inibitore orale covalente ITK/JAK3 per la dermatite atopica da moderata a grave. Sono forniti due documenti: l'Esibizione 99.1 (presentazione per gli investitori) e l'Esibizione 99.2 (comunicato stampa). Secondo il Regolamento FD, gli elementi 7.01 e 8.01 sono forniti, ma non archiviati, quindi le informazioni non sono soggette alla responsabilità ai sensi dell'Exchange Act né incorporate automaticamente in altri rapporti SEC.

Il modulo 8-K non contiene dati numerici sull'efficacia, la sicurezza o metriche finanziarie. Gli investitori devono consultare gli allegati o partecipare alla conference call per i risultati dettagliati. Non sono incluse modifiche ai bilanci o alle precedenti previsioni.

Aclaris Therapeutics (Nasdaq: ACRS) ha presentado un Formulario 8-K para informar a los inversores que realizará una llamada conferencia el 29 de julio de 2025 para revisar los datos preliminares de su estudio de Fase 2a de ATI-2138, un inhibidor oral covalente ITK/JAK3 para dermatitis atópica de moderada a grave. Se proporcionan dos elementos: Anexo 99.1 (presentación para inversores) y Anexo 99.2 (comunicado de prensa). Bajo el Reglamento FD, los ítems 7.01 y 8.01 se proporcionan pero no se presentan oficialmente, por lo que la información no está sujeta a responsabilidad según la Exchange Act ni se incorpora automáticamente en otros informes de la SEC.

El 8-K no contiene métricas numéricas de eficacia, seguridad o financieras. Los inversores deben consultar los anexos o unirse a la llamada conferencia para obtener resultados detallados. No se incluyen cambios en estados financieros ni en guías previamente emitidas.

Aclaris Therapeutics (나스닥: ACRS)는 2025년 7월 29일에 중등도에서 중증 아토피 피부염 치료를 위한 경구용 공유 결합 ITK/JAK3 억제제 ATI-2138의 2a상 연구 주요 결과를 검토하는 컨퍼런스 콜을 개최할 예정임을 투자자에게 알리기 위해 Form 8-K를 제출했습니다. 두 가지 자료가 제공됩니다: 전시물 99.1(투자자 프레젠테이션)과 전시물 99.2(보도자료). Reg FD에 따라 항목 7.01 및 8.01은 제출된 것이 아니라 제공된 것이므로, 이 정보는 Exchange Act 책임 대상이 아니며 다른 SEC 보고서에 자동으로 포함되지 않습니다.

8-K 문서에는 수치상의 효능, 안전성 또는 재무 지표가 포함되어 있지 않습니다. 투자자들은 자세한 결과를 위해 첨부 자료를 참조하거나 컨퍼런스 콜에 참여해야 합니다. 재무제표나 이전 가이드라인의 변경 사항은 포함되어 있지 않습니다.

Aclaris Therapeutics (Nasdaq : ACRS) a déposé un formulaire 8-K pour informer les investisseurs qu’elle organisera une conférence téléphonique le 29 juillet 2025 afin de passer en revue les données principales de son étude de phase 2a sur ATI-2138, un inhibiteur oral covalent ITK/JAK3 pour la dermatite atopique modérée à sévère. Deux éléments sont fournis : Annexe 99.1 (présentation aux investisseurs) et Annexe 99.2 (communiqué de presse). En vertu du règlement FD, les éléments 7.01 et 8.01 sont fournis mais non déposés, ce qui signifie que ces informations ne sont pas soumises à la responsabilité selon l’Exchange Act et ne sont pas automatiquement intégrées dans d’autres rapports SEC.

Le formulaire 8-K ne contient aucune donnée chiffrée sur l’efficacité, la sécurité ou les indicateurs financiers. Les investisseurs doivent consulter les annexes ou participer à la conférence téléphonique pour obtenir des résultats détaillés. Aucun changement aux états financiers ou aux prévisions précédemment publiées n’est inclus.

Aclaris Therapeutics (Nasdaq: ACRS) hat ein Formular 8-K eingereicht, um Investoren darüber zu informieren, dass am 29. Juli 2025 eine Telefonkonferenz stattfinden wird, in der die Topline-Daten der Phase-2a-Studie zu ATI-2138, einem oralen kovalenten ITK/JAK3-Inhibitor für mittelschwere bis schwere atopische Dermatitis, vorgestellt werden. Zwei Anlagen werden bereitgestellt: Anlage 99.1 (Investorpräsentation) und Anlage 99.2 (Pressemitteilung). Gemäß Regulation FD werden die Punkte 7.01 und 8.01 bereitgestellt, aber nicht eingereicht, sodass die Informationen nicht der Haftung nach dem Exchange Act unterliegen und nicht automatisch in andere SEC-Berichte aufgenommen werden.

Das 8-K enthält keine numerischen Angaben zu Wirksamkeit, Sicherheit oder finanziellen Kennzahlen. Investoren müssen die beigefügten Anlagen konsultieren oder an der Telefonkonferenz teilnehmen, um detaillierte Ergebnisse zu erhalten. Änderungen an Finanzberichten oder zuvor veröffentlichten Prognosen sind nicht enthalten.

Positive
  • Announcement of top-line Phase 2a results for ATI-2138 signals ongoing development progress and upcoming clinical visibility.
Negative
  • Filing lacks any efficacy or safety data, leaving investors unable to gauge clinical success or valuation impact.

Insights

TL;DR: Filing announces forthcoming Phase 2a data; impact indeterminate until actual numbers released.

Pipeline progress matters in biotech valuations, and ATI-2138’s emergence from Phase 2a is a gating event. However, the 8-K omits efficacy or safety readouts, preventing assessment of clinical or commercial viability. Investors should withhold judgment until Exhibit 99.2 is reviewed or management comments on response rates, pruritus scores and adverse events.

TL;DR: Procedural 8-K; no immediate valuation catalyst without data.

The filing satisfies Reg FD by alerting the market to an upcoming disclosure. Because the information is furnished, it does not trigger SEC liability or automatic inclusion in future filings. Absent quantitative results, share-price impact is likely muted until the press release or call provides clarity on trial success, timeline to Phase 3 and funding needs.

Aclaris Therapeutics (Nasdaq: ACRS) ha presentato un modulo 8-K per informare gli investitori che terrà una conference call il 29 luglio 2025 per esaminare i dati preliminari del suo studio di Fase 2a su ATI-2138, un inibitore orale covalente ITK/JAK3 per la dermatite atopica da moderata a grave. Sono forniti due documenti: l'Esibizione 99.1 (presentazione per gli investitori) e l'Esibizione 99.2 (comunicato stampa). Secondo il Regolamento FD, gli elementi 7.01 e 8.01 sono forniti, ma non archiviati, quindi le informazioni non sono soggette alla responsabilità ai sensi dell'Exchange Act né incorporate automaticamente in altri rapporti SEC.

Il modulo 8-K non contiene dati numerici sull'efficacia, la sicurezza o metriche finanziarie. Gli investitori devono consultare gli allegati o partecipare alla conference call per i risultati dettagliati. Non sono incluse modifiche ai bilanci o alle precedenti previsioni.

Aclaris Therapeutics (Nasdaq: ACRS) ha presentado un Formulario 8-K para informar a los inversores que realizará una llamada conferencia el 29 de julio de 2025 para revisar los datos preliminares de su estudio de Fase 2a de ATI-2138, un inhibidor oral covalente ITK/JAK3 para dermatitis atópica de moderada a grave. Se proporcionan dos elementos: Anexo 99.1 (presentación para inversores) y Anexo 99.2 (comunicado de prensa). Bajo el Reglamento FD, los ítems 7.01 y 8.01 se proporcionan pero no se presentan oficialmente, por lo que la información no está sujeta a responsabilidad según la Exchange Act ni se incorpora automáticamente en otros informes de la SEC.

El 8-K no contiene métricas numéricas de eficacia, seguridad o financieras. Los inversores deben consultar los anexos o unirse a la llamada conferencia para obtener resultados detallados. No se incluyen cambios en estados financieros ni en guías previamente emitidas.

Aclaris Therapeutics (나스닥: ACRS)는 2025년 7월 29일에 중등도에서 중증 아토피 피부염 치료를 위한 경구용 공유 결합 ITK/JAK3 억제제 ATI-2138의 2a상 연구 주요 결과를 검토하는 컨퍼런스 콜을 개최할 예정임을 투자자에게 알리기 위해 Form 8-K를 제출했습니다. 두 가지 자료가 제공됩니다: 전시물 99.1(투자자 프레젠테이션)과 전시물 99.2(보도자료). Reg FD에 따라 항목 7.01 및 8.01은 제출된 것이 아니라 제공된 것이므로, 이 정보는 Exchange Act 책임 대상이 아니며 다른 SEC 보고서에 자동으로 포함되지 않습니다.

8-K 문서에는 수치상의 효능, 안전성 또는 재무 지표가 포함되어 있지 않습니다. 투자자들은 자세한 결과를 위해 첨부 자료를 참조하거나 컨퍼런스 콜에 참여해야 합니다. 재무제표나 이전 가이드라인의 변경 사항은 포함되어 있지 않습니다.

Aclaris Therapeutics (Nasdaq : ACRS) a déposé un formulaire 8-K pour informer les investisseurs qu’elle organisera une conférence téléphonique le 29 juillet 2025 afin de passer en revue les données principales de son étude de phase 2a sur ATI-2138, un inhibiteur oral covalent ITK/JAK3 pour la dermatite atopique modérée à sévère. Deux éléments sont fournis : Annexe 99.1 (présentation aux investisseurs) et Annexe 99.2 (communiqué de presse). En vertu du règlement FD, les éléments 7.01 et 8.01 sont fournis mais non déposés, ce qui signifie que ces informations ne sont pas soumises à la responsabilité selon l’Exchange Act et ne sont pas automatiquement intégrées dans d’autres rapports SEC.

Le formulaire 8-K ne contient aucune donnée chiffrée sur l’efficacité, la sécurité ou les indicateurs financiers. Les investisseurs doivent consulter les annexes ou participer à la conférence téléphonique pour obtenir des résultats détaillés. Aucun changement aux états financiers ou aux prévisions précédemment publiées n’est inclus.

Aclaris Therapeutics (Nasdaq: ACRS) hat ein Formular 8-K eingereicht, um Investoren darüber zu informieren, dass am 29. Juli 2025 eine Telefonkonferenz stattfinden wird, in der die Topline-Daten der Phase-2a-Studie zu ATI-2138, einem oralen kovalenten ITK/JAK3-Inhibitor für mittelschwere bis schwere atopische Dermatitis, vorgestellt werden. Zwei Anlagen werden bereitgestellt: Anlage 99.1 (Investorpräsentation) und Anlage 99.2 (Pressemitteilung). Gemäß Regulation FD werden die Punkte 7.01 und 8.01 bereitgestellt, aber nicht eingereicht, sodass die Informationen nicht der Haftung nach dem Exchange Act unterliegen und nicht automatisch in andere SEC-Berichte aufgenommen werden.

Das 8-K enthält keine numerischen Angaben zu Wirksamkeit, Sicherheit oder finanziellen Kennzahlen. Investoren müssen die beigefügten Anlagen konsultieren oder an der Telefonkonferenz teilnehmen, um detaillierte Ergebnisse zu erhalten. Änderungen an Finanzberichten oder zuvor veröffentlichten Prognosen sind nicht enthalten.

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UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, DC 20549

 

FORM 8-K

 

CURRENT REPORT

PURSUANT TO SECTION 13 OR 15(D) OF THE

SECURITIES EXCHANGE ACT OF 1934

 

Date of report (Date of earliest event reported): July 29, 2025

 

Phibro Animal Health Corporation

(EXACT NAME OF REGISTRANT AS SPECIFIED IN CHARTER)

 

Delaware   01-36410   13-1840497
(State or other jurisdiction
of incorporation)
  (Commission File Number)   (IRS Employer Identification No.)

 

Glenpointe Centre East, 3rd Floor

300 Frank W. Burr Boulevard, Suite 21

Teaneck, New Jersey 07666-6712

(Address of Principal Executive Offices, including Zip Code)

 

(201) 329-7300

(Registrant’s telephone number, including area code)

 

Not Applicable

(Former name or former address, if changed since last report)

 

Securities registered pursuant to Section 12(b) of the Act:

 

Title of each class   Trading Symbol(s)   Name of each exchange on which registered
Class A Common Stock, $0.0001 par value per share   PAHC   NASDAQ Stock Market

 

Check the appropriate box below if this Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:

 

¨Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)

 

¨Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)

 

¨Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))

 

¨Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))

  

Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (17 CFR §230.405) or Rule 12b-2 of the Securities Exchange Act of 1934 (17 CFR §240.12b-2).

 

Emerging growth company ¨

 

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ¨

 

 

 

 

 

 

ITEM 8.01 OTHER EVENTS

 

On July 29, 2025, Phibro Animal Health Corporation issued a press release announcing the declaration of a quarterly cash dividend of $0.12 per share on its Class A common stock and Class B common stock, payable on September 24, 2025, to stockholders of record at the close of business on September 3, 2025. A copy of the press release announcing the dividend is filed as Exhibit 99.1 to this Current Report on Form 8-K and is incorporated herein by reference.

 

ITEM 9.01 FINANCIAL STATEMENTS AND EXHIBITS.

 

(d) Exhibits

 

Exhibit
Number
  Description
     
99.1   Press Release, dated July 29, 2025.
     
104   Cover Page Interactive Data File (embedded within the Inline XBRL document).

 

 

 

 

SIGNATURES

 

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned thereunto duly authorized.

 

PHIBRO ANIMAL HEALTH CORPORATION
 Registrant
Date: July 29, 2025 
  
 By: /s/ Judith Weinstein
 Name: Judith Weinstein
 Title: Senior Vice President, General Counsel and Corporate Secretary

 

 

 

FAQ

What did Aclaris Therapeutics (ACRS) announce in its 8-K?

The company disclosed it will discuss top-line Phase 2a results for ATI-2138 during a 29 Jul 2025 conference call and issued related exhibits.

Is the actual ATI-2138 Phase 2a data included in the filing?

No. The 8-K references a presentation (Ex. 99.1) and press release (Ex. 99.2); the filing itself contains no numerical results.

What is ATI-2138?

ATI-2138 is an investigational oral covalent ITK/JAK3 inhibitor being studied for moderate-to-severe atopic dermatitis.

Are the furnished materials considered "filed" with the SEC?

No. Under Reg FD, Items 7.01 and 8.01 are furnished, not filed, and are not subject to Exchange Act liability.

Will this 8-K affect Aclaris’s financial statements?

The filing contains no financial statements or guidance updates, so existing financials remain unchanged.
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