Jasper Therapeutics Reports Second Quarter 2024 Financial Results and Recent Corporate Developments
Jasper Therapeutics (Nasdaq: JSPR) reported Q2 2024 financial results and corporate updates. Key highlights include:
1. Faster-than-expected enrollment in BEACON and SPOTLIGHT studies for briquilimab in chronic urticaria.
2. Additional 180mg Q8W dosing cohort added to BEACON study.
3. Initial data from BEACON study (up to 240mg dosing) expected in Q4 2024.
4. Expanded mast cell portfolio with new asthma program.
5. Q2 2024 financials: $106.8M cash on hand, $11.3M R&D expenses, $4.7M G&A expenses, $15.0M net loss ($0.97 per share).
The company remains optimistic about briquilimab's potential in mast cell-driven diseases and plans to present initial data from both BEACON and SPOTLIGHT studies later this year.
Jasper Therapeutics (Nasdaq: JSPR) ha riportato i risultati finanziari del secondo trimestre 2024 e aggiornamenti aziendali. I punti salienti includono:
1. Arruolamento più veloce del previsto negli studi BEACON e SPOTLIGHT per il briquilimab nella forma cronica di orticaria.
2. Aggiunta di un ulteriore coorte di dosaggio da 180mg ogni 8 settimane nello studio BEACON.
3. I dati iniziali dallo studio BEACON (fino a 240mg di dosaggio) sono attesi nel quarto trimestre del 2024.
4. Espansione del portafoglio di mastociti con un nuovo programma contro l'asma.
5. Finanziari del secondo trimestre 2024: $106.8M di liquidità, $11.3M di spese per R&S, $4.7M di spese generali e amministrative, $15.0M di perdita netta ($0.97 per azione).
L'azienda rimane ottimista riguardo al potenziale del briquilimab nelle malattie guidate dai mastociti e prevede di presentare i dati iniziali sia dagli studi BEACON che SPOTLIGHT entro la fine dell'anno.
Jasper Therapeutics (Nasdaq: JSPR) informó los resultados financieros del segundo trimestre de 2024 y actualizaciones corporativas. Los puntos destacados incluyen:
1. Inscripción más rápida de lo esperado en los estudios BEACON y SPOTLIGHT para el briquilimab en la urticaria crónica.
2. Se agregó un nuevo grupo de dosificación de 180mg cada 8 semanas en el estudio BEACON.
3. Se esperan los datos iniciales del estudio BEACON (hasta 240mg de dosificación) para el cuarto trimestre de 2024.
4. Ampliación de la cartera de mastocitos con un nuevo programa para el asma.
5. Financieros del segundo trimestre de 2024: $106.8M en efectivo, $11.3M en gastos de I+D, $4.7M en gastos generales y administrativos, $15.0M en pérdida neta ($0.97 por acción).
La empresa se mostró optimista acerca del potencial del briquilimab en enfermedades impulsadas por mastocitos y planea presentar datos iniciales de los estudios BEACON y SPOTLIGHT más adelante este año.
재스퍼 치료제(Jasper Therapeutics)(Nasdaq: JSPR)가 2024년 2분기 재무 결과 및 기업 업데이트를 발표했습니다. 주요 사항은 다음과 같습니다:
1. 만성 두드러기에 대한 브리퀼리맙(briquilimab)의 BEACON 및 SPOTLIGHT 연구에서 예상보다 빠른 환자 등록.
2. BEACON 연구에 180mg Q8W 투약 그룹 추가.
3. BEACON 연구(최대 240mg 투약)에서 초기 데이터는 2024년 4분기에 발표될 예정.
4. 새로운 천식 프로그램으로 마스트세포 포트폴리오 확장.
5. 2024년 2분기 재무: 현금 1억 680만 달러, 연구개발 비용 1천130만 달러, 일반 관리 비용 470만 달러, 순손실 1천500만 달러($0.97 per share).
회사는 마스트세포로 유도되는 질병에서 브리퀼리맙의 잠재력에 대해 낙관적이며, 올해 말까지 BEACON 및 SPOTLIGHT 연구의 초기 데이터를 발표할 계획입니다.
Jasper Therapeutics (Nasdaq: JSPR) a annoncé les résultats financiers du deuxième trimestre 2024 et des mises à jour d'entreprise. Les faits marquants incluent :
1. Une inscription plus rapide que prévu dans les études BEACON et SPOTLIGHT pour le briquilimab dans l'urticaire chronique.
2. Ajout d'un groupe de dosage supplémentaire de 180 mg toutes les 8 semaines à l'étude BEACON.
3. Les premières données de l'étude BEACON (jusqu'à 240 mg de dosage) devraient être disponibles au quatrième trimestre 2024.
4. Portefeuille de mastocytes élargi avec un nouveau programme sur l'asthme.
5. Finances du deuxième trimestre 2024 : 106,8 millions de dollars en liquidités, 11,3 millions de dollars de dépenses en R&D, 4,7 millions de dollars de dépenses générales et administratives, 15 millions de dollars de perte nette (0,97 $ par action).
L'entreprise reste optimiste quant au potentiel du briquilimab dans les maladies à médiation mastocytaire et prévoit de présenter les premières données des études BEACON et SPOTLIGHT plus tard cette année.
Jasper Therapeutics (Nasdaq: JSPR) hat die finanziellen Ergebnisse des zweiten Quartals 2024 und Unternehmensaktualisierungen bekannt gegeben. Zu den wichtigsten Punkten gehören:
1. Schnellere als erwartete Rekrutierung in den Studien BEACON und SPOTLIGHT für Briquilimab bei chronischer Urtikaria.
2. Hinzufügen einer weiteren Dosierungsgruppe von 180 mg alle 8 Wochen zur BEACON-Studie.
3. Erste Daten aus der BEACON-Studie (bis zu 240 mg Dosierung) werden im vierten Quartal 2024 erwartet.
4. Erweiterung des Mastzellportfolios mit einem neuen Asthma-Programm.
5. Finanzielle Ergebnisse des zweiten Quartals 2024: 106,8 Millionen US-Dollar an liquiden Mitteln, 11,3 Millionen US-Dollar an F&E-Ausgaben, 4,7 Millionen US-Dollar an allgemeinen Verwaltungskosten, 15,0 Millionen US-Dollar Nettoverlust (0,97 US-Dollar pro Aktie).
Das Unternehmen bleibt optimistisch hinsichtlich des Potenzials von Briquilimab bei mastzellbasierten Erkrankungen und plant, noch in diesem Jahr erste Daten aus den Studien BEACON und SPOTLIGHT zu präsentieren.
- Faster-than-expected enrollment in BEACON and SPOTLIGHT studies
- Addition of 180mg Q8W dosing cohort to BEACON study for more robust dataset
- Expansion of mast cell portfolio with new asthma program
- Strong cash position of $106.8 million as of June 30, 2024
- Net loss of $15.0 million for Q2 2024
- Increased R&D expenses of $11.3 million in Q2 2024
Insights
Jasper Therapeutics' Q2 2024 results reveal a mixed financial picture. While the company reported a net loss of
R&D expenses of
However, the lack of revenue and ongoing losses highlight the speculative nature of this clinical-stage biotech investment. Investors should closely monitor cash burn rate and potential future financing needs.
The accelerated enrollment in BEACON and SPOTLIGHT studies for briquilimab is a positive signal, potentially indicating strong interest from both patients and clinicians. The addition of a new dosing cohort (180mg Q8W) in the BEACON study demonstrates flexibility in trial design and could provide valuable insights for optimal dosing strategies.
The planned data readout in Q4 2024, including UAS7 scores, UCT scores and serum tryptase levels, will be crucial in assessing briquilimab's efficacy. The expansion into asthma further broadens the potential applications of briquilimab, leveraging its mast cell-targeting mechanism.
Preclinical data presented at EAACI 2024 showing briquilimab's potential in asthma and atopic dermatitis adds depth to the pipeline. However, investors should remember that preclinical success doesn't guarantee clinical efficacy.
Jasper Therapeutics' focus on mast cell-driven diseases with briquilimab positions them in a potentially lucrative niche. The rapid progress in clinical trials, particularly in CSU and CIndU, could accelerate their path to market if positive results are achieved.
The expansion into asthma broadens their addressable market significantly. With
The appointment of Dr. Svetlana Lucas to the board strengthens their strategic planning and business development capabilities, which will be crucial for future partnering or commercialization efforts.
However, investors should note that Jasper faces competition from established players in the allergy and asthma space. The company's success will depend on briquilimab's efficacy and safety profile compared to existing treatments.
Enrollment in BEACON and SPOTLIGHT studies progressing faster than expected; enrollment in the 240mg single-dose cohort of the BEACON study ongoing
Additional dosing cohort (180mg Q8W) added to BEACON study
Initial data from BEACON study through 240mg dosing cohort to be presented in 4Q24
REDWOOD CITY, Calif., Aug. 13, 2024 (GLOBE NEWSWIRE) -- Jasper Therapeutics, Inc. (Nasdaq: JSPR) (Jasper), a clinical stage biotechnology company focused on development of briquilimab, a novel antibody therapy targeting c-Kit (CD117) to address mast cell driven diseases such as chronic spontaneous urticaria (CSU), chronic inducible urticaria (CIndU) and asthma, today announced results for the fiscal quarter ended June 30, 2024, reported recent corporate developments, and provided an update on progress in the BEACON and SPOTLIGHT studies.
“We have continued to make excellent progress advancing briquilimab during the second quarter, with patient enrollment proceeding faster than initially expected in the BEACON and SPOTLIGHT studies,” said Ronald Martell, President and Chief Executive Officer of Jasper. “The strong rate of enrollment has given us the opportunity to include additional cohorts in our initial CSU data readout, and we are now planning to present results from dosing cohorts up to 240mg in the fourth quarter of this year. While the company remains blinded to efficacy data from the study, rapid enrollment in BEACON has also given us the flexibility to expand the study to include an additional dosing cohort evaluating briquilimab at 180mg Q8W. This will enable us to generate a more robust dataset to support dose selection for our planned registrational trials in CSU without impacting their timelines.”
“We are very pleased with the progress in the BEACON and SPOTLIGHT studies thus far,” said Edwin Tucker, M.D., Chief Medical Officer of Jasper. “With the support of our investigators, the efforts of the Jasper team and the timely review and approval by the Independent Data Monitoring Committee (IDMC) we have been able to quickly proceed through dose escalation on the BEACON study and are now enrolling patients at the highest dose, 240mg. This rapid progress and safety affirmation by the IDMC has enabled expansion of the BEACON study to obtain more clinical insights into the potential benefits of briquilimab for patients with CSU, without delaying the program. We look forward to reviewing and presenting initial data from both the BEACON and SPOTLIGHT studies later this year, followed in early 2025 by the full study reports to be presented at a medical conference.”
Highlights for Second Quarter 2024 and Recent Weeks
- Completed enrollment in the 80mg Q8W, the 120mg Q8W, the 120mg Q12W and the 180mg Q12W cohorts of the BEACON study in CSU. As of August 13th, 2024, the 240mg, single dose cohort is actively enrolling patients and the newly added 180mg, Q8W cohort is expected to be open for enrollment imminently. Jasper has opened 31 clinical sites in the BEACON study across the U.S. and EU to date.
- Based on the favorable rate of enrollment in the BEACON study, Jasper is now planning to report data from all dosing cohorts initially included in the study in the fourth quarter of 2024, and continued enrollment at the current pace would allow for the inclusion of the recently added 180mg Q8W cohort in the initial data disclosure as well. Endpoints that the company expects to disclose in the readout include UAS7 scores, UCT scores, serum tryptase, and adverse events. Efficacy data from the study remains blinded to the Company until the interim analysis associated with the initial data readout.
- Expanded the Company’s Phase 1b/2a BEACON study in CSU with the addition of a cohort evaluating 180mg of briquilimab (N=8) administered on an 8-week dosing schedule. The BEACON study is a dose escalation trial evaluating repeat doses of subcutaneous briquilimab in adult CSU patients who remain symptomatic after treatment with, or who cannot tolerate, omalizumab. Parts 2 and 3 of the study are double-blind and placebo controlled, and the Company remains blinded to all efficacy data in the study until the initial data analysis is conducted, currently planned for the fourth quarter of 2024.
- Enrollment is ongoing in the second cohort (120mg) of the Company’s Phase 1b/2a SPOTLIGHT study in CIndU. The SPOTLIGHT study is evaluating a single administration of subcutaneous briquilimab in adult patients with cold urticaria (ColdU) or symptomatic dermographism (SD). Jasper anticipates reporting initial data from the SPOTLIGHT study in the fourth quarter of 2024.
- Announced the expansion of the Company’s mast cell portfolio with a new development program in asthma and hosted a KOL webinar on the potential of briquilimab in the indication. Jasper expects to begin enrolling patients in a Phase 1b/2a study in patients with asthma in the fourth quarter of 2024.
- Announced the appointment of Svetlana Lucas, Ph.D., to Jasper’s Board of Directors; Dr. Lucas adds particular expertise in strategic planning and business development to the Company’s Board.
- Presented preclinical data demonstrating the effect of briquilimab on hematopoietic stem cells at the European Hematology Association (EHA) Hybrid Congress; the presented study evaluated the molecular basis of inhibition of the stem cell factor (SCF)/c-Kit signaling pathway via briquilimab and its functional impact on healthy human HSC survival, proliferation, and differentiation. Results from the study demonstrate that blocking of SCF/c-Kit signaling by briquilimab does not cause apoptosis of HSCs, and that HSCs cultured in the presence of briquilimab differentiate directly into CD34- cells with higher c-Kit expression and without increased CD38 expression.
- Presented data from preclinical and healthy volunteer studies of briquilimab, as well as trial-in-progress presentations from its BEACON and SPOTLIGHT clinical studies, at the EAACI Congress 2024.
- The two preclinical studies presented showed the potential of briquilimab in asthma and atopic dermatitis (AD), respectively. The asthma study demonstrated that a single dose of briquilimab can deplete mast cells in both inflamed and non-inflamed tissue as well as improve lung function in an allergen-induced asthma model. In the AD study, treatment with briquilimab led to a reduction of dermal mast cells and inflammatory leukocytes, indicating that mast cells play a critical role in the pathogenesis of AD and that briquilimab has the potential to reverse AD pathology by depleting those cells. Both preclinical studies utilized Jasper’s proprietary c-Kit Mouse™, which overcomes the limitations of standard models that do not bind antibodies directed at the human c-Kit receptor.
- Jasper also presented data from the previously disclosed clinical study of briquilimab in healthy volunteers showing that it has a promising safety profile, appears to be well-tolerated, exhibits a favorable pharmacokinetic (PK) profile, and leads to sustained and dose-dependent depletion of mast cells in a cutaneous wound model. The PK and pharmacodynamic (PD) profiles demonstrated in the study support dose selection for Jasper’s ongoing BEACON and SPOTLIGHT clinical trials in CSU and CIndU.
Second Quarter Fiscal 2024 Financial Results
- Cash and cash equivalents as of June 30, 2024, totaled
$106.8 million . - Research and development expenses for the quarter ended June 30, 2024, were
$11.3 million , including stock-based compensation expenses of$0.5 million . - General and administrative expenses for the quarter ended June 30, 2024, were
$4.7 million , including stock-based compensation expenses of$1.0 million . - Jasper reported a net loss of
$15.0 million , or basic and diluted net loss per share attributable to common stockholders of$0.97 , for the quarter ended June 30, 2024.
About Briquilimab
Briquilimab (formerly JSP191) is a targeted aglycosylated monoclonal antibody that blocks stem cell factor from binding to the cell-surface receptor c-Kit, also known as CD117, thereby inhibiting signaling through the receptor. This inhibition disrupts the critical survival signal, leading to the depletion of the mast cells via apoptosis which removes the underlying source of the inflammatory response in mast cell driven diseases such as chronic urticaria. Jasper is currently conducting clinical studies of briquilimab as a treatment in patients with CSU or with CIndU and is planning to initiate a clinical study in patients with asthma. Briquilimab is also currently in clinical studies as a treatment for patients with LR-MDS and as a conditioning agent for cell therapies for rare diseases. To date, briquilimab has a demonstrated efficacy and safety profile in more than 145 dosed participants and healthy volunteers, with clinical outcomes as a conditioning agent in severe combined immunodeficiency (SCID), acute myeloid leukemia (AML), myelodysplastic syndromes (MDS), Fanconi anemia (FA), and sickle cell disease (SCD).
About Jasper
Jasper is a clinical-stage biotechnology company developing briquilimab, a monoclonal antibody targeting c-Kit (CD117) as a therapeutic for chronic mast and stem cell diseases such as chronic urticaria, asthma and lower to intermediate risk MDS and as a conditioning agent for stem cell transplants for rare diseases such as SCD, FA and SCID. To date, briquilimab has a demonstrated efficacy and safety profile in more than 145 dosed participants and healthy volunteers, with clinical outcomes as a conditioning agent in SCID, AML, MDS, FA, and SCD. For more information, please visit us at www.jaspertherapeutics.com.
Forward-Looking Statements
Certain statements included in this press release that are not historical facts are forward-looking statements for purposes of the safe harbor provisions under the United States Private Securities Litigation Reform Act of 1995. Forward-looking statements are sometimes accompanied by words such as “believe,” “may,” “will,” “estimate,” “continue,” “anticipate,” “intend,” “expect,” “should,” “would,” “plan,” “predict,” “potential,” “seem,” “seek,” “future,” “outlook” and similar expressions that predict or indicate future events or trends or that are not statements of historical matters. These forward-looking statements include, but are not limited to, statements regarding briquilimab’s potential, including with respect to its potential in mast cell driven diseases such as CSU, CIndU, and asthma, its ability to block SCF/c-Kit signaling and not cause apoptosis of HSCs, the potential for HSCs cultured in the presence of briquilimab to differentiate directly into CD34- cells with higher c-Kit expression and without increased CD38 expression, a single dose’s ability to deplete mast cells in both inflamed and non-inflamed tissue as well as improve lung function in an allergen-induced asthma model, its potential to lead to a reduction of dermal mast cells and inflammatory leukocytes in AD and its potential to reverse AD pathology by depleting those cells, its potential to lead to sustained and dose-dependent depletion of mast cells in a cutaneous wound model, and the promising safety profile of briquilimab in mast cell diseases; Jasper’s expectations regarding its BEACON study, including expected patient enrollment, additional cohorts, expected timing for presentation of data, expected endpoints to be disclosed in the initial readout, including UAS7 scores, UCT scores, serum tryptase, and adverse events, expected expansion of the study, expected generation of a more robust dataset to support dose selection, expected clinical insights into the potential benefits of briquilimab for patients with CSU, the Company’s expectation that the initial data readout for the BEACON will cover up to the 240mg dosing cohort, including the 180mg Q8W cohort, and the planned presentation of the full study report at a medical conference in 2025; Jasper’s expectations regarding its SPOTLIGHT study, including patient enrollment, expected timing for reporting initial data and planned presentation of the full study report at a medical conference in 2025; Jasper’s expectations regarding its planned registration trials in CSU; and Jasper’s expectations regarding a Phase 1b/2a study in asthma patients, including expecting timing of patient enrollment. These statements are based on various assumptions, whether or not identified in this press release, and on the current expectations of Jasper and are not predictions of actual performance. These forward-looking statements are provided for illustrative purposes only and are not intended to serve as, and must not be relied on by an investor as, a guarantee, an assurance, a prediction or a definitive statement of fact or probability. Many actual events and circumstances are beyond the control of Jasper. These forward-looking statements are subject to a number of risks and uncertainties, including general economic, political and business conditions; the risk that the potential product candidates that Jasper develops may not progress through clinical development or receive required regulatory approvals within expected timelines or at all; the risk that clinical trials may not confirm any safety, potency or other product characteristics described or assumed in this press release; the risk that Jasper will be unable to successfully market or gain market acceptance of its product candidates; the risk that prior study results may not be replicated; the risk that Jasper’s product candidates may not be beneficial to patients or successfully commercialized; patients’ willingness to try new therapies and the willingness of physicians to prescribe these therapies; the effects of competition on Jasper’s business; the risk that third parties on which Jasper depends for laboratory, clinical development, manufacturing and other critical services will fail to perform satisfactorily; the risk that Jasper’s business, operations, clinical development plans and timelines, and supply chain could be adversely affected by the effects of health epidemics; the risk that Jasper will be unable to obtain and maintain sufficient intellectual property protection for its investigational products or will infringe the intellectual property protection of others; and other risks and uncertainties indicated from time to time in Jasper’s filings with the SEC, including its Annual Report on Form 10-K for the year ended December 31, 2023 and subsequent Quarterly Reports on Form 10-Q. If any of these risks materialize or Jasper’s assumptions prove incorrect, actual results could differ materially from the results implied by these forward-looking statements. While Jasper may elect to update these forward-looking statements at some point in the future, Jasper specifically disclaims any obligation to do so. These forward-looking statements should not be relied upon as representing Jasper’s assessments of any date subsequent to the date of this press release. Accordingly, undue reliance should not be placed upon the forward-looking statements.
Contacts:
Joyce Allaire (investors)
LifeSci Advisors
617-435-6602
jallaire@lifesciadvisors.com
Alex Gray (investors)
Jasper Therapeutics
650-549-1454
agray@jaspertherapeutics.com
Lauren Walker (media)
Real Chemistry
646-564-2156
lbarbiero@realchemistry.com
| JASPER THERAPEUTICS, INC. | |||||||||||||||
| CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS | |||||||||||||||
| (in thousands, except share and per share data) | |||||||||||||||
| (unaudited) | |||||||||||||||
| Three Months Ended June 30, | Six Months Ended June 30, | ||||||||||||||
| 2024 | 2023 | 2024 | 2023 | ||||||||||||
| Operating expenses | |||||||||||||||
| Research and development(1) | $ | 11,296 | $ | 13,297 | $ | 21,594 | $ | 23,102 | |||||||
| General and administrative(1) | 4,697 | 4,530 | 9,471 | 8,672 | |||||||||||
| Total operating expenses | 15,993 | 17,827 | 31,065 | 31,774 | |||||||||||
| Loss from operations | (15,993 | ) | (17,827 | ) | (31,065 | ) | (31,774 | ) | |||||||
| Interest income | 1,450 | 1,436 | 2,836 | 2,532 | |||||||||||
| Change in fair value of earnout liability | — | 420 | (20 | ) | (344 | ) | |||||||||
| Change in fair value of common stock warrant liability | — | — | — | (575 | ) | ||||||||||
| Other expense, net | (40 | ) | (109 | ) | (62 | ) | (179 | ) | |||||||
| Total other income, net | 1,410 | 1,747 | 2,754 | 1,434 | |||||||||||
| Net loss and comprehensive loss | $ | (14,583 | ) | $ | (16,080 | ) | $ | (28,311 | ) | $ | (30,340 | ) | |||
| Net loss per share attributable to common stockholders, basic and diluted | $ | (0.97 | ) | $ | (1.47 | ) | $ | (2.00 | ) | $ | (3.08 | ) | |||
| Weighted-average shares used in computing net loss per share attributable to common stockholders, basic and diluted | 14,986,367 | 10,921,239 | 14,160,634 | 9,860,392 | |||||||||||
| (1) Amounts include non-cash stock based compensation expense as follows (in thousands): | |||||||||||||||
| Three Months Ended June 30, | Six Months Ended June 30, | ||||||||||||||
| 2024 | 2023 | 2024 | 2023 | ||||||||||||
| Research and development | $ | 473 | $ | 491 | $ | 822 | $ | 959 | |||||||
| General and administrative | 1,009 | 900 | 1,829 | 1,699 | |||||||||||
| Total | $ | 1,482 | $ | 1,391 | $ | 2,651 | $ | 2,658 | |||||||
| JASPER THERAPEUTICS, INC. | |||||||
| CONDENSED CONSOLIDATED BALANCE SHEETS | |||||||
| (in thousands) | |||||||
| (unaudited) | |||||||
| June 30, | December 31, | ||||||
| Assets | 2024 | 2023 | |||||
| Current assets: | |||||||
| Cash and cash equivalents | $ | 106,819 | $ | 86,887 | |||
| Prepaid expenses and other current assets | 1,861 | 2,051 | |||||
| Total current assets | 108,680 | 88,938 | |||||
| Property and equipment, net | 2,438 | 2,727 | |||||
| Operating lease right-of-use assets | 1,231 | 1,467 | |||||
| Restricted cash | 417 | 417 | |||||
| Other non-current assets | 1,163 | 1,343 | |||||
| Total assets | $ | 113,929 | $ | 94,892 | |||
| Liabilities and Stockholders’ Equity | |||||||
| Current liabilities: | |||||||
| Accounts payable | $ | 2,964 | $ | 4,149 | |||
| Current portion of operating lease liabilities | 1,029 | 972 | |||||
| Earnout liability | 20 | - | |||||
| Accrued expenses and other current liabilities | 6,055 | 7,253 | |||||
| Total current liabilities | 10,068 | 12,374 | |||||
| Non-current portion of operating lease liabilities | 1,287 | 1,814 | |||||
| Other non-current liabilities | 2,264 | 2,264 | |||||
| Total liabilities | 13,619 | 16,452 | |||||
| Commitments and contingencies | |||||||
| Stockholders’ equity: | |||||||
| Preferred stock | — | — | |||||
| Common stock | 2 | 1 | |||||
| Additional paid-in capital | 298,219 | 248,039 | |||||
| Accumulated deficit | (197,911 | ) | (169,600 | ) | |||
| Total stockholders’ equity | 100,310 | 78,440 | |||||
| Total liabilities and stockholders’ equity | $ | 113,929 | $ | 94,892 | |||
FAQ
What are the key clinical trials for Jasper Therapeutics' briquilimab?
When will Jasper Therapeutics (JSPR) report initial data from the BEACON study?
What new development program did Jasper Therapeutics announce in Q2 2024?
What was Jasper Therapeutics' (JSPR) cash position as of June 30, 2024?
