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Crinetics Pharmaceuticals, Inc. (CRNX) filed a Form 8-K under Item 7.01 (Regulation FD). The filing discloses that the company issued a press release announcing eight scientific abstracts from its endocrine and rare-disease pipeline that will be presented at the Endocrine Society’s Annual Meeting (ENDO 2025) in San Francisco, July 12-15, 2025.

The abstracts will cover development candidates atumelnant (ACTH antagonist), paltusotine (oral SST2 agonist), and the TSHR antagonist CRN12755. The company also reiterates plans for the potential commercial launch of PALSONIFY (commercial name for paltusotine) if regulatory approval is obtained.

No new clinical data, financial figures, or transaction details are provided in the 8-K; the disclosure is limited to notification of the upcoming presentations. All forward-looking statements are qualified by customary risk factors, including clinical, regulatory, and geopolitical uncertainties.

Crinetics Pharmaceuticals, Inc. (CRNX) ha presentato un modulo 8-K sotto la voce Item 7.01 (Regulation FD). Nel documento viene annunciato che la società ha diffuso un comunicato stampa riguardante otto abstract scientifici dal suo portafoglio di endocrinologia e malattie rare, che saranno presentati al Congresso Annuale della Endocrine Society (ENDO 2025) a San Francisco, dal 12 al 15 luglio 2025.

Gli abstract riguarderanno i candidati in sviluppo atumelnant (antagonista ACTH), paltusotine (agonista SST2 orale) e l'antagonista TSHR CRN12755. La società ribadisce inoltre i piani per un possibile lancio commerciale di PALSONIFY (nome commerciale di paltusotine) qualora venga ottenuta l'approvazione regolatoria.

Nel modulo 8-K non sono forniti nuovi dati clinici, informazioni finanziarie o dettagli sulle transazioni; la comunicazione è limitata all’annuncio delle prossime presentazioni. Tutte le dichiarazioni previsionali sono soggette ai consueti fattori di rischio, inclusi quelli clinici, regolatori e geopolitici.

Crinetics Pharmaceuticals, Inc. (CRNX) presentó un Formulario 8-K bajo el ítem 7.01 (Regulation FD). El documento revela que la compañía emitió un comunicado de prensa anunciando ocho resúmenes científicos de su línea de endocrinología y enfermedades raras que serán presentados en la Reunión Anual de la Endocrine Society (ENDO 2025) en San Francisco, del 12 al 15 de julio de 2025.

Los resúmenes cubrirán los candidatos en desarrollo atumelnant (antagonista ACTH), paltusotine (agonista oral SST2) y el antagonista TSHR CRN12755. La empresa también reitera sus planes para un posible lanzamiento comercial de PALSONIFY (nombre comercial de paltusotine) si se obtiene la aprobación regulatoria.

El 8-K no incluye nuevos datos clínicos, cifras financieras ni detalles de transacciones; la divulgación se limita a notificar las próximas presentaciones. Todas las declaraciones prospectivas están sujetas a factores de riesgo habituales, incluyendo incertidumbres clínicas, regulatorias y geopolíticas.

Crinetics Pharmaceuticals, Inc. (CRNX)는 Item 7.01 (Regulation FD)에 따라 Form 8-K를 제출했습니다. 해당 문서에는 회사가 내분비 및 희귀질환 파이프라인에서 여덟 개의 과학 초록을 발표하는 보도자료를 배포했으며, 이 초록들이 2025년 7월 12일부터 15일까지 샌프란시스코에서 열리는 내분비학회 연례회의(ENDO 2025)에서 발표될 예정임이 공개되어 있습니다.

초록들은 개발 중인 후보물질 atumelnant (ACTH 길항제), paltusotine (경구 SST2 작용제), 그리고 TSHR 길항제 CRN12755를 다룰 예정입니다. 또한 회사는 규제 승인 시 PALSONIFY (paltusotine의 상업명)의 잠재적 상업 출시 계획을 재확인했습니다.

8-K 문서에는 새로운 임상 데이터, 재무 수치 또는 거래 세부사항이 포함되어 있지 않으며, 공개 내용은 다가오는 발표에 대한 알림에 한정됩니다. 모든 미래 예측 진술은 임상, 규제, 지정학적 불확실성 등 일반적인 위험 요소에 의해 제한됩니다.

Crinetics Pharmaceuticals, Inc. (CRNX) a déposé un formulaire 8-K sous l’item 7.01 (Regulation FD). Ce dépôt révèle que la société a publié un communiqué de presse annonçant huit résumés scientifiques issus de son portefeuille en endocrinologie et maladies rares, qui seront présentés lors de la réunion annuelle de l’Endocrine Society (ENDO 2025) à San Francisco, du 12 au 15 juillet 2025.

Les résumés porteront sur les candidats en développement atumelnant (antagoniste ACTH), paltusotine (agoniste oral SST2) et l’antagoniste TSHR CRN12755. La société réaffirme également ses projets de lancement commercial potentiel de PALSONIFY (nom commercial de paltusotine) si une approbation réglementaire est obtenue.

Aucune nouvelle donnée clinique, information financière ou détail de transaction n’est fourni dans ce 8-K ; la communication se limite à l’annonce des prochaines présentations. Toutes les déclarations prospectives sont soumises aux facteurs de risque habituels, incluant les incertitudes cliniques, réglementaires et géopolitiques.

Crinetics Pharmaceuticals, Inc. (CRNX) hat ein Formular 8-K unter Punkt 7.01 (Regulation FD) eingereicht. Die Einreichung gibt bekannt, dass das Unternehmen eine Pressemitteilung veröffentlicht hat, in der acht wissenschaftliche Abstracts aus seiner Endokrinologie- und Seltene-Krankheiten-Pipeline angekündigt werden, die auf der Jahrestagung der Endocrine Society (ENDO 2025) in San Francisco vom 12. bis 15. Juli 2025 vorgestellt werden.

Die Abstracts behandeln die Entwicklungskandidaten atumelnant (ACTH-Antagonist), paltusotine (oraler SST2-Agonist) und den TSHR-Antagonisten CRN12755. Das Unternehmen bekräftigt außerdem seine Pläne für einen möglichen kommerziellen Start von PALSONIFY (Handelsname für paltusotine), sofern eine behördliche Zulassung erteilt wird.

Im 8-K werden keine neuen klinischen Daten, Finanzzahlen oder Transaktionsdetails angegeben; die Offenlegung beschränkt sich auf die Ankündigung der bevorstehenden Präsentationen. Alle zukunftsgerichteten Aussagen unterliegen den üblichen Risikofaktoren, einschließlich klinischer, regulatorischer und geopolitischer Unsicherheiten.

Positive
  • Eight abstracts accepted for ENDO 2025, demonstrating breadth and continued progress across multiple endocrine programs.
  • Multiple pipeline candidates highlighted (atumelnant, paltusotine, CRN12755), keeping investor attention on diversified clinical assets.
Negative
  • No new clinical or financial data were disclosed, limiting immediate valuation impact.
  • Forward-looking statements emphasize numerous development and regulatory risks without providing mitigating updates.

Insights

TL;DR – Pipeline visibility rises, but no new data; limited market impact.

The 8-K merely alerts investors to forthcoming scientific presentations. While announcing eight abstracts does signal an active R&D engine spanning atumelnant, paltusotine, and a TSHR antagonist, the lack of fresh efficacy or safety readouts keeps valuation unchanged for now. Investors will look to ENDO 2025 data for potential inflection points, particularly around paltusotine’s commercial readiness and CRN12755’s first-in-human progress. Absent those results, today’s filing is informational and non-material.

TL;DR – Disclosure highlights standard development risks; impact neutral.

The company reiterates numerous forward-looking statements and risk factors common to clinical-stage biopharma: trial timing, regulatory review, supply-chain disruption, and data variability. Because no new commitments or financial obligations arise from the ENDO 2025 participation, downside or upside risk profile is unchanged.

Crinetics Pharmaceuticals, Inc. (CRNX) ha presentato un modulo 8-K sotto la voce Item 7.01 (Regulation FD). Nel documento viene annunciato che la società ha diffuso un comunicato stampa riguardante otto abstract scientifici dal suo portafoglio di endocrinologia e malattie rare, che saranno presentati al Congresso Annuale della Endocrine Society (ENDO 2025) a San Francisco, dal 12 al 15 luglio 2025.

Gli abstract riguarderanno i candidati in sviluppo atumelnant (antagonista ACTH), paltusotine (agonista SST2 orale) e l'antagonista TSHR CRN12755. La società ribadisce inoltre i piani per un possibile lancio commerciale di PALSONIFY (nome commerciale di paltusotine) qualora venga ottenuta l'approvazione regolatoria.

Nel modulo 8-K non sono forniti nuovi dati clinici, informazioni finanziarie o dettagli sulle transazioni; la comunicazione è limitata all’annuncio delle prossime presentazioni. Tutte le dichiarazioni previsionali sono soggette ai consueti fattori di rischio, inclusi quelli clinici, regolatori e geopolitici.

Crinetics Pharmaceuticals, Inc. (CRNX) presentó un Formulario 8-K bajo el ítem 7.01 (Regulation FD). El documento revela que la compañía emitió un comunicado de prensa anunciando ocho resúmenes científicos de su línea de endocrinología y enfermedades raras que serán presentados en la Reunión Anual de la Endocrine Society (ENDO 2025) en San Francisco, del 12 al 15 de julio de 2025.

Los resúmenes cubrirán los candidatos en desarrollo atumelnant (antagonista ACTH), paltusotine (agonista oral SST2) y el antagonista TSHR CRN12755. La empresa también reitera sus planes para un posible lanzamiento comercial de PALSONIFY (nombre comercial de paltusotine) si se obtiene la aprobación regulatoria.

El 8-K no incluye nuevos datos clínicos, cifras financieras ni detalles de transacciones; la divulgación se limita a notificar las próximas presentaciones. Todas las declaraciones prospectivas están sujetas a factores de riesgo habituales, incluyendo incertidumbres clínicas, regulatorias y geopolíticas.

Crinetics Pharmaceuticals, Inc. (CRNX)는 Item 7.01 (Regulation FD)에 따라 Form 8-K를 제출했습니다. 해당 문서에는 회사가 내분비 및 희귀질환 파이프라인에서 여덟 개의 과학 초록을 발표하는 보도자료를 배포했으며, 이 초록들이 2025년 7월 12일부터 15일까지 샌프란시스코에서 열리는 내분비학회 연례회의(ENDO 2025)에서 발표될 예정임이 공개되어 있습니다.

초록들은 개발 중인 후보물질 atumelnant (ACTH 길항제), paltusotine (경구 SST2 작용제), 그리고 TSHR 길항제 CRN12755를 다룰 예정입니다. 또한 회사는 규제 승인 시 PALSONIFY (paltusotine의 상업명)의 잠재적 상업 출시 계획을 재확인했습니다.

8-K 문서에는 새로운 임상 데이터, 재무 수치 또는 거래 세부사항이 포함되어 있지 않으며, 공개 내용은 다가오는 발표에 대한 알림에 한정됩니다. 모든 미래 예측 진술은 임상, 규제, 지정학적 불확실성 등 일반적인 위험 요소에 의해 제한됩니다.

Crinetics Pharmaceuticals, Inc. (CRNX) a déposé un formulaire 8-K sous l’item 7.01 (Regulation FD). Ce dépôt révèle que la société a publié un communiqué de presse annonçant huit résumés scientifiques issus de son portefeuille en endocrinologie et maladies rares, qui seront présentés lors de la réunion annuelle de l’Endocrine Society (ENDO 2025) à San Francisco, du 12 au 15 juillet 2025.

Les résumés porteront sur les candidats en développement atumelnant (antagoniste ACTH), paltusotine (agoniste oral SST2) et l’antagoniste TSHR CRN12755. La société réaffirme également ses projets de lancement commercial potentiel de PALSONIFY (nom commercial de paltusotine) si une approbation réglementaire est obtenue.

Aucune nouvelle donnée clinique, information financière ou détail de transaction n’est fourni dans ce 8-K ; la communication se limite à l’annonce des prochaines présentations. Toutes les déclarations prospectives sont soumises aux facteurs de risque habituels, incluant les incertitudes cliniques, réglementaires et géopolitiques.

Crinetics Pharmaceuticals, Inc. (CRNX) hat ein Formular 8-K unter Punkt 7.01 (Regulation FD) eingereicht. Die Einreichung gibt bekannt, dass das Unternehmen eine Pressemitteilung veröffentlicht hat, in der acht wissenschaftliche Abstracts aus seiner Endokrinologie- und Seltene-Krankheiten-Pipeline angekündigt werden, die auf der Jahrestagung der Endocrine Society (ENDO 2025) in San Francisco vom 12. bis 15. Juli 2025 vorgestellt werden.

Die Abstracts behandeln die Entwicklungskandidaten atumelnant (ACTH-Antagonist), paltusotine (oraler SST2-Agonist) und den TSHR-Antagonisten CRN12755. Das Unternehmen bekräftigt außerdem seine Pläne für einen möglichen kommerziellen Start von PALSONIFY (Handelsname für paltusotine), sofern eine behördliche Zulassung erteilt wird.

Im 8-K werden keine neuen klinischen Daten, Finanzzahlen oder Transaktionsdetails angegeben; die Offenlegung beschränkt sich auf die Ankündigung der bevorstehenden Präsentationen. Alle zukunftsgerichteten Aussagen unterliegen den üblichen Risikofaktoren, einschließlich klinischer, regulatorischer und geopolitischer Unsicherheiten.

SEC Form 4
FORM 4 UNITED STATES SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549

STATEMENT OF CHANGES IN BENEFICIAL OWNERSHIP

Filed pursuant to Section 16(a) of the Securities Exchange Act of 1934
or Section 30(h) of the Investment Company Act of 1940
OMB APPROVAL
OMB Number: 3235-0287
Estimated average burden
hours per response: 0.5
Check this box if no longer subject to Section 16. Form 4 or Form 5 obligations may continue. See Instruction 1(b).
Check this box to indicate that a transaction was made pursuant to a contract, instruction or written plan for the purchase or sale of equity securities of the issuer that is intended to satisfy the affirmative defense conditions of Rule 10b5-1(c). See Instruction 10.
1. Name and Address of Reporting Person*
Schmidt Kurt

(Last) (First) (Middle)
1 CAMPBELL PLACE

(Street)
CAMDEN NJ 08103

(City) (State) (Zip)
2. Issuer Name and Ticker or Trading Symbol
CAMPBELL'S Co [ CPB ]
5. Relationship of Reporting Person(s) to Issuer
(Check all applicable)
X Director 10% Owner
Officer (give title below) Other (specify below)
3. Date of Earliest Transaction (Month/Day/Year)
06/26/2025
4. If Amendment, Date of Original Filed (Month/Day/Year)
6. Individual or Joint/Group Filing (Check Applicable Line)
X Form filed by One Reporting Person
Form filed by More than One Reporting Person
Table I - Non-Derivative Securities Acquired, Disposed of, or Beneficially Owned
1. Title of Security (Instr. 3) 2. Transaction Date (Month/Day/Year) 2A. Deemed Execution Date, if any (Month/Day/Year) 3. Transaction Code (Instr. 8) 4. Securities Acquired (A) or Disposed Of (D) (Instr. 3, 4 and 5) 5. Amount of Securities Beneficially Owned Following Reported Transaction(s) (Instr. 3 and 4) 6. Ownership Form: Direct (D) or Indirect (I) (Instr. 4) 7. Nature of Indirect Beneficial Ownership (Instr. 4)
Code V Amount (A) or (D) Price
Table II - Derivative Securities Acquired, Disposed of, or Beneficially Owned
(e.g., puts, calls, warrants, options, convertible securities)
1. Title of Derivative Security (Instr. 3) 2. Conversion or Exercise Price of Derivative Security 3. Transaction Date (Month/Day/Year) 3A. Deemed Execution Date, if any (Month/Day/Year) 4. Transaction Code (Instr. 8) 5. Number of Derivative Securities Acquired (A) or Disposed of (D) (Instr. 3, 4 and 5) 6. Date Exercisable and Expiration Date (Month/Day/Year) 7. Title and Amount of Securities Underlying Derivative Security (Instr. 3 and 4) 8. Price of Derivative Security (Instr. 5) 9. Number of derivative Securities Beneficially Owned Following Reported Transaction(s) (Instr. 4) 10. Ownership Form: Direct (D) or Indirect (I) (Instr. 4) 11. Nature of Indirect Beneficial Ownership (Instr. 4)
Code V (A) (D) Date Exercisable Expiration Date Title Amount or Number of Shares
Phantom Stock (1) 06/26/2025 A 2,309.43 (2) (3) Common Stock 2,309.43 $0 44,633.8(4) D
Explanation of Responses:
1. Each share of Phantom Stock is the economic equivalent of one share of issuer common stock.
2. Phantom shares are fully vested.
3. The value of Phantom Stock is payable in cash from the Company's Supplemental Retirement Plan upon reporting person's retirement, resignation or termination.
4. Includes 455.60 shares acquired through dividend reinvestment since the reporting person's last report.
Remarks:
Ex 24 - Power of Attorney
Marci K. Donnelly, Attorney-in-Fact 06/30/2025
** Signature of Reporting Person Date
Reminder: Report on a separate line for each class of securities beneficially owned directly or indirectly.
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FAQ

When will Crinetics (CRNX) present its ENDO 2025 abstracts?

The presentations are scheduled for July 12-15, 2025, at the Endocrine Society’s annual meeting in San Francisco.

How many abstracts is Crinetics presenting at ENDO 2025?

The company will present eight abstracts covering several pipeline programs.

Which pipeline programs are included in the ENDO 2025 abstracts?

Abstracts will feature atumelnant, paltusotine, and the TSHR antagonist CRN12755.

Does the 8-K contain new clinical results for paltusotine or atumelnant?

No. The filing only announces upcoming presentations and contains no new efficacy or safety data.

What is PALSONIFY mentioned in the filing?

PALSONIFY is the proposed commercial name for paltusotine, which Crinetics plans to launch if regulatory approval is granted.
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