OmniAb Reports Fourth Quarter and Full Year 2024 Financial Results and Business Highlights
OmniAb (NASDAQ: OABI) reported its Q4 and full-year 2024 financial results. Q4 revenue increased to $10.8 million from $4.8 million in Q3 2023, while full-year 2024 revenue decreased to $26.4 million from $34.2 million in 2023. The company reported a Q4 net loss of $13.1 million ($0.12 per share) and a full-year net loss of $62.0 million ($0.61 per share).
As of December 31, 2024, OmniAb had 91 active partners and 363 active programs, including 32 OmniAb-derived programs in clinical development or commercialization. The company signed 10 new license agreements in 2024. For 2025, OmniAb projects revenue between $20-25 million and operating expenses of $90-95 million.
The company launched OmniHub™, a unified interface for partners to access discovery campaign data. Notable partner developments include Immunovant's IMVT-1402 progress, with six IND applications cleared, and various clinical advancements in partner programs including batoclimab, acasunlimab, and sugemalimab.
OmniAb (NASDAQ: OABI) ha riportato i risultati finanziari del Q4 e dell'intero anno 2024. I ricavi del Q4 sono aumentati a 10,8 milioni di dollari rispetto ai 4,8 milioni di dollari del Q3 2023, mentre i ricavi dell'intero anno 2024 sono diminuiti a 26,4 milioni di dollari rispetto ai 34,2 milioni di dollari del 2023. L'azienda ha registrato una perdita netta nel Q4 di 13,1 milioni di dollari (0,12 dollari per azione) e una perdita netta per l'intero anno di 62,0 milioni di dollari (0,61 dollari per azione).
Al 31 dicembre 2024, OmniAb aveva 91 partner attivi e 363 programmi attivi, inclusi 32 programmi derivati da OmniAb in fase di sviluppo clinico o commercializzazione. L'azienda ha firmato 10 nuovi accordi di licenza nel 2024. Per il 2025, OmniAb prevede ricavi tra 20 e 25 milioni di dollari e spese operative tra 90 e 95 milioni di dollari.
L'azienda ha lanciato OmniHub™, un'interfaccia unificata per i partner per accedere ai dati delle campagne di scoperta. Sviluppi significativi dei partner includono i progressi di Immunovant con IMVT-1402, con sei domande IND approvate, e vari avanzamenti clinici nei programmi dei partner tra cui batoclimab, acasunlimab e sugemalimab.
OmniAb (NASDAQ: OABI) reportó sus resultados financieros del cuarto trimestre y del año completo 2024. Los ingresos del cuarto trimestre aumentaron a 10.8 millones de dólares desde 4.8 millones de dólares en el tercer trimestre de 2023, mientras que los ingresos del año completo 2024 disminuyeron a 26.4 millones de dólares desde 34.2 millones de dólares en 2023. La compañía reportó una pérdida neta en el cuarto trimestre de 13.1 millones de dólares (0.12 dólares por acción) y una pérdida neta para el año completo de 62.0 millones de dólares (0.61 dólares por acción).
Al 31 de diciembre de 2024, OmniAb tenía 91 socios activos y 363 programas activos, incluidos 32 programas derivados de OmniAb en desarrollo clínico o comercialización. La compañía firmó 10 nuevos acuerdos de licencia en 2024. Para 2025, OmniAb proyecta ingresos entre 20 y 25 millones de dólares y gastos operativos de 90 a 95 millones de dólares.
La compañía lanzó OmniHub™, una interfaz unificada para que los socios accedan a los datos de las campañas de descubrimiento. Los desarrollos notables de socios incluyen los avances de Immunovant con IMVT-1402, con seis solicitudes IND aprobadas, y varios avances clínicos en programas de socios, incluidos batoclimab, acasunlimab y sugemalimab.
OmniAb (NASDAQ: OABI)는 2024년 4분기 및 전체 연도 재무 결과를 발표했습니다. 4분기 매출은 2023년 3분기의 480만 달러에서 1,080만 달러로 증가했으며, 2024년 전체 연도 매출은 2023년의 3,420만 달러에서 2,640만 달러로 감소했습니다. 회사는 4분기 순손실이 1,310만 달러(주당 0.12 달러)이며, 전체 연도 순손실이 6,200만 달러(주당 0.61 달러)라고 보고했습니다.
2024년 12월 31일 기준으로 OmniAb는 91개의 활성 파트너와 363개의 활성 프로그램을 보유하고 있으며, 이 중 32개는 임상 개발 또는 상용화 중인 OmniAb 유래 프로그램입니다. 회사는 2024년에 10개의 새로운 라이선스 계약을 체결했습니다. 2025년에는 OmniAb가 2천만에서 2천5백만 달러의 매출과 9천만에서 9천5백만 달러의 운영 비용을 예상하고 있습니다.
회사는 파트너가 발견 캠페인 데이터를 접근할 수 있는 통합 인터페이스인 OmniHub™를 출시했습니다. 주목할 만한 파트너 개발에는 Immunovant의 IMVT-1402 진행 상황이 포함되며, 6개의 IND 신청이 승인되었고, batoclimab, acasunlimab 및 sugemalimab을 포함한 파트너 프로그램에서 다양한 임상 발전이 이루어졌습니다.
OmniAb (NASDAQ: OABI) a publié ses résultats financiers pour le quatrième trimestre et l'année complète 2024. Les revenus du quatrième trimestre ont augmenté à 10,8 millions de dollars contre 4,8 millions de dollars au troisième trimestre 2023, tandis que les revenus de l'année complète 2024 ont diminué à 26,4 millions de dollars contre 34,2 millions de dollars en 2023. La société a enregistré une perte nette de 13,1 millions de dollars (0,12 dollar par action) pour le quatrième trimestre et une perte nette de 62,0 millions de dollars (0,61 dollar par action) pour l'année complète.
Au 31 décembre 2024, OmniAb comptait 91 partenaires actifs et 363 programmes actifs, dont 32 programmes dérivés d'OmniAb en développement clinique ou en commercialisation. L'entreprise a signé 10 nouveaux accords de licence en 2024. Pour 2025, OmniAb prévoit des revenus compris entre 20 et 25 millions de dollars et des dépenses d'exploitation de 90 à 95 millions de dollars.
L'entreprise a lancé OmniHub™, une interface unifiée permettant aux partenaires d'accéder aux données des campagnes de découverte. Les développements notables des partenaires incluent les progrès d'Immunovant avec l'IMVT-1402, avec six demandes IND approuvées, ainsi que divers avancements cliniques dans les programmes des partenaires, y compris batoclimab, acasunlimab et sugemalimab.
OmniAb (NASDAQ: OABI) hat seine Finanzzahlen für das 4. Quartal und das gesamte Jahr 2024 veröffentlicht. Der Umsatz im 4. Quartal stieg auf 10,8 Millionen Dollar von 4,8 Millionen Dollar im 3. Quartal 2023, während der Umsatz für das gesamte Jahr 2024 auf 26,4 Millionen Dollar von 34,2 Millionen Dollar im Jahr 2023 zurückging. Das Unternehmen berichtete über einen Nettoverlust im 4. Quartal von 13,1 Millionen Dollar (0,12 Dollar pro Aktie) und einen Nettoverlust für das gesamte Jahr von 62,0 Millionen Dollar (0,61 Dollar pro Aktie).
Zum 31. Dezember 2024 hatte OmniAb 91 aktive Partner und 363 aktive Programme, darunter 32 Programme, die aus OmniAb stammen und sich in der klinischen Entwicklung oder Kommerzialisierung befinden. Das Unternehmen unterzeichnete 10 neue Lizenzvereinbarungen im Jahr 2024. Für 2025 prognostiziert OmniAb einen Umsatz zwischen 20 und 25 Millionen Dollar sowie Betriebskosten von 90 bis 95 Millionen Dollar.
Das Unternehmen hat OmniHub™ gestartet, eine einheitliche Schnittstelle für Partner, um auf Daten von Entdeckungskampagnen zuzugreifen. Bemerkenswerte Partnerentwicklungen umfassen Immunovants Fortschritte mit IMVT-1402, bei denen sechs IND-Anträge genehmigt wurden, sowie verschiedene klinische Fortschritte in Partnerprogrammen, darunter batoclimab, acasunlimab und sugemalimab.
- Q4 2024 revenue increased 125% year-over-year to $10.8 million
- Signed 10 new license agreements in 2024
- 91 active partners and 363 active programs, with 32 in clinical development/commercialization
- Launched new OmniHub™ technology platform
- Multiple partner programs advancing in clinical trials
- Full-year 2024 revenue decreased 23% to $26.4 million from $34.2 million in 2023
- Net loss increased to $62.0 million in 2024 from $50.6 million in 2023
- Royalty revenue decreased due to lower partner product sales
- 2025 revenue guidance ($20-25M) below 2024 actual revenue ($26.4M)
Insights
OmniAb's Q4 2024 results present a mixed financial picture with some encouraging signs for future growth. Q4 revenue grew impressively to
The company showed improved cost control with reduced R&D expenses (
The 2025 guidance suggests management expects relatively flat revenue performance (
The business metrics show strong momentum with 91 active partners (double-digit percentage growth) and 363 active programs, including 32 in clinical development or commercialization. The addition of 10 new licensing agreements and 5 new antibodies entering clinical trials in 2024 demonstrates the platform's continued adoption and potential for future milestone/royalty revenue.
OmniAb's partner program advancements highlight the company's growing importance in antibody discovery. The progress across multiple partner assets demonstrates the platform's versatility across different therapeutic areas and antibody formats.
Immunovant's rapid advancement of IMVT-1402 with six IND clearances and enrollment in pivotal Phase 2b studies for Graves' disease and rheumatoid arthritis represents significant progress. Their ambitious plan to initiate trials in 10 indications by March 2026 could significantly expand the market opportunity if successful.
The batoclimab program (another Immunovant asset) is approaching several important data readouts in myasthenia gravis and chronic inflammatory demyelinating polyneuropathy by Q1 2025. Its Orphan Drug Designation in Japan for thyroid eye disease enhances its commercial potential in that market.
Genmab's acasunlimab entering Phase 3 for second-line NSCLC treatment represents advancement into a commercially significant indication. Similarly, CStone's publication of positive Phase 3 results for sugemalimab in gastric cancer in JAMA validates the clinical significance of their findings, with meaningful survival benefits in PD-L1 positive patients.
The early-stage pipeline also shows promise, with Aptevo's mipletamig achieving 100% remission in the initial cohort for acute myeloid leukemia, and Rondo's RNDO-564 demonstrating activity in antibody-drug-conjugate-resistant bladder cancer models. These emerging programs could represent significant future value drivers if clinical development continues successfully.
Conference Call with Slides Begins at 4:30 p.m. Eastern Time Today
“2024 was a remarkable year featuring double-digit percentage growth in the number of both active partners and programs. Clinical-stage programs advanced well, and we launched new technologies and enhancements that strengthened our platform and expanded our reach,” said Matt Foehr, Chief Executive Officer of OmniAb. “We exceeded our internal goals for key metrics and continued to build momentum while optimizing the scalability of our business. We believe our commitment to innovation is a significant competitive advantage and creates exciting opportunities for future growth. We remain steadfast in our strategic direction and are excited about the prospects that lie ahead.”
Fourth Quarter 2024 Financial Results
Revenue for the fourth quarter of 2024 was
Research and development expense was
Net loss for the fourth quarter of 2024 was
Full Year 2024 Financial Results
Revenue for 2024 was
Research and development expense for 2024 was
Net loss for 2024 was
As of December 31, 2024, OmniAb had cash, cash equivalents and short-term investments of
2025 Financial Guidance
OmniAb today introduced 2025 financial guidance. OmniAb expects 2025 revenue to be in the range of
Fourth Quarter 2024 and Recent Business Highlights
As of December 31, 2024, OmniAb had 91 active partners and 363 active programs, including 32 OmniAb-derived programs in clinical development or being commercialized. The Company signed 10 new license agreements in 2024, including two in the fourth quarter with Incyte Corporation and Photinia Biosciences. In addition, five new OmniAb-derived antibodies entered the clinic in 2024.
In December 2024, OmniAb launched OmniHub™, a unified interface designed to provide partners with secure access to datasets to visualize their discovery campaign data with a variety of custom tools. This bioinformatics portal is designed to enable scalable and secure data transfer, advanced visualization and computational tool access.
Fourth quarter 2024 and recent partner highlights include the following:
IMVT-1402
- Immunovant announced that its lead asset, IMVT-1402, is rapidly progressing with six Investigational New Drug (IND) applications now cleared and pivotal Phase 2b studies in Graves’ disease (GD) and difficult-to-treat rheumatoid arthritis now enrolling.
- Immunovant is on track to initiate potentially registrational programs for three additional indications for IMVT-1402 by March 31, 2025. In addition, Immunovant anticipates initiating clinical trials evaluating IMVT-1402 in a total of 10 indications by March 31, 2026.
Batoclimab
- Immunovant reported that the top-line results of the batoclimab trial in myasthenia gravis and the initial results from period 1 of the batoclimab trial in chronic inflammatory demyelinating polyneuropathy are expected by March 31, 2025.
- Immunovant also plans to announce additional data from the batoclimab proof-of-concept study in GD, including six-month, treatment-free remission data in the summer 2025.
- Additionally, Immunovant reported that top-line results from the pivotal program of batoclimab for the treatment of thyroid eye disease (TED), also known as Graves' ophthalmopathy, are expected in the second half of 2025.
- HanAll Biopharma announced that batoclimab has received Orphan Drug Designation from Japan’s Ministry of Health, Labor, and Welfare for active TED.
Acasunlimab
- Genmab announced that a Phase 3 trial with acasunlimab as a second-line therapy in non-small cell lung cancer (NSCLC) is now enrolling patients and that they expect to provide an additional Phase 2 data update in NSCLC in 2025.
Zimberelimab
- Arcus Biosciences expects to present overall survival (OS) data from the Phase 2 EDGE-Gastric study, which is evaluating domvanalimab plus zimberelimab and chemotherapy in upper gastrointestinal adenocarcinomas, in the fall of 2025.
- Arcus Biosciences also expects to initiate three new expansion cohorts within the Phase 1/1b ARC-20 study in the first quarter of 2025, including one cohort for casdatifan plus zimberelimab in all-comer first-line clear cell renal cell carcinoma.
Sugemalimab
- CStone announced the publication of the Phase 3 GEMSTONE-303 study results for sugemalimab in patients with unresectable locally advanced or metastatic G/GEJ adenocarcinoma in the Journal of the American Medical Association. Results showed that in patients with PD-L1 combined positive score ≥5, sugemalimab significantly improved both OS and progression-free survival (PFS) compared with the control group. Median OS was 15.6 months versus 12.6 months, and median PFS was 7.6 months versus 6.1 months.
-
CStone announced that they have entered into a strategic partnership with Pharmalink Store for commercialization of sugemalimab in the
Middle East ,North Africa andSouth Africa . Additionally, CStone has partnered with SteinCares to market sugemalimab inLatin America .
Mipletamig
-
Aptevo Therapeutics announced that
100% of patients in Cohort 1 of the mipletamig RAINIER Phase 1b/2 dose-optimization trial for frontline acute myeloid leukemia achieved remission within 30 days of treatment. Trial enrollment is ongoing. Aptevo also anticipates providing multiple data readouts in 2025 and presenting results at the American Society of Hematology meeting in the fourth quarter of 2025.
RNDO-564
- Rondo Therapeutics presented data from preclinical studies of RNDO-564, a novel CD28 x Nectin-4 costimulatory bispecific antibody for advanced bladder cancer, at the 2025 American Society of Clinical Oncology Genitourinary Cancers Symposium. RNDO-564 demonstrated robust anti-tumor activity in vivo and in vitro, including in an antibody-drug-conjugate-resistant bladder cancer model. Based on promising preclinical findings, Rondo is advancing RNDO-564 through IND-enabling studies and expects to initiate a Phase 1/b trial in relapsed/refractory, locally advanced/metastatic bladder cancer by year-end 2025.
Conference Call and Webcast
OmniAb management will host a conference call with accompanying slides today beginning at 4:30 p.m. Eastern time (1:30 p.m. Pacific time) to discuss this announcement and answer questions. To participate via telephone, please dial (800) 549-8228 using the conference ID 84579. Slides, as well as the live and replay webcast of the call, are available at https://investors.omniab.com/investors/events-and-presentations/default.aspx.
About OmniAb®
OmniAb licenses cutting edge discovery research technology to pharmaceutical and biotech companies and academic institutions to enable the discovery of next-generation therapeutics. Our technology platform creates and screens diverse antibody repertoires and is designed to quickly identify optimal antibodies and other target-binding proteins for our partners’ drug development efforts. At the heart of the OmniAb platform is something we call Biological Intelligence™, which powers the immune systems of our proprietary, engineered transgenic animals to create optimized antibody candidates for human therapeutics. We believe the OmniAb animals comprise the most diverse host systems available in the industry. Our suite of technologies and methods, including computational antigen design and immunization methods, paired with high-throughput single B cell phenotypic screening and mining of next-generation sequencing datasets with custom algorithms, is used to identify fully-human antibodies with exceptional performance and developability characteristics. We provide our partners both integrated end-to-end capabilities and highly customizable offerings, which address critical industry challenges and provide optimized discovery solutions. Our business model aligns scientific and economic interests of our partners through structured agreements that generally include upfront/access fees, service revenue, milestones and royalties on commercial sales.
For more information, please visit www.omniab.com.
Forward-Looking Statements
OmniAb cautions you that statements contained in this press release regarding matters that are not historical facts are forward-looking statements. Words such as “may,” “will,” “should,” “expect,” “plan,” “anticipate,” “could,” “intend,” “target,” “project,” “contemplates,” “believes,” “estimates,” “predicts,” “potential” or continue” and similar expressions, are intended to identify forward-looking statements. The forward-looking statements are based on our current beliefs and expectations and include, but are not limited to: statements regarding our competitive advantage and the growth prospects of our business; the scalability of our business; the expected performance of our technologies and the opportunities they may create; the ability to add new partners and programs; scientific presentations and clinical and regulatory events of our partners and the timing thereof; and our 2025 financial guidance. Actual results may differ from those set forth in this press release due to the risks and uncertainties inherent in our business, including, without limitation: our future success is dependent on acceptance of our technology platform and technologies by new and existing partners, as well as on the eventual development, approval and commercialization of products developed by our partners for which we have no control over the development plan, regulatory strategy or commercialization efforts; biopharmaceutical development is inherently uncertain; risks arising from changes in technology; the competitive environment in the life sciences and biotechnology platform market; our failure to maintain, protect and defend our intellectual property rights; difficulties with performance of third parties we will rely on for our business; regulatory developments in
Partner Information
The information in this press release regarding partnered products and programs comes from information publicly released by our partners.
[Tables Follow]
OMNIAB, INC. |
|||||||
CONSOLIDATED BALANCE SHEETS |
|||||||
(unaudited, in thousands, except share and per share data) |
|||||||
|
December 31, |
||||||
|
2024 |
|
2023 |
||||
ASSETS |
|
|
|
||||
Current assets: |
|
|
|
||||
Cash and cash equivalents |
$ |
27,598 |
|
|
$ |
16,358 |
|
Short-term investments |
|
31,836 |
|
|
|
70,625 |
|
Accounts receivable, net |
|
5,272 |
|
|
|
3,844 |
|
Prepaid expenses and other current assets |
|
3,432 |
|
|
|
4,074 |
|
Total current assets |
|
68,138 |
|
|
|
94,901 |
|
Intangible assets, net |
|
138,060 |
|
|
|
155,467 |
|
Goodwill |
|
83,979 |
|
|
|
83,979 |
|
Property and equipment, net |
|
15,492 |
|
|
|
18,249 |
|
Operating lease right-of-use assets |
|
17,789 |
|
|
|
19,884 |
|
Restricted cash |
|
560 |
|
|
|
560 |
|
Other long-term assets |
|
1,540 |
|
|
|
2,185 |
|
Total assets |
$ |
325,558 |
|
|
$ |
375,225 |
|
LIABILITIES AND STOCKHOLDERS’ EQUITY |
|
|
|
||||
Current liabilities: |
|
|
|
||||
Accounts payable |
$ |
2,297 |
|
|
$ |
4,411 |
|
Accrued expenses and other current liabilities |
|
6,141 |
|
|
|
7,068 |
|
Current contingent liabilities |
|
531 |
|
|
|
1,303 |
|
Current deferred revenue |
|
2,337 |
|
|
|
6,848 |
|
Current operating lease liabilities |
|
3,782 |
|
|
|
3,486 |
|
Total current liabilities |
|
15,088 |
|
|
|
23,116 |
|
Long-term contingent liabilities |
|
953 |
|
|
|
3,203 |
|
Deferred income taxes, net |
|
2,314 |
|
|
|
11,354 |
|
Long-term operating lease liabilities |
|
19,382 |
|
|
|
22,075 |
|
Long-term deferred revenue |
|
117 |
|
|
|
862 |
|
Other long-term liabilities |
|
86 |
|
|
|
30 |
|
Total liabilities |
|
37,940 |
|
|
|
60,640 |
|
Stockholders’ equity: |
|
|
|
||||
Preferred stock, |
|
— |
|
|
|
— |
|
Common stock, |
|
12 |
|
|
|
12 |
|
Additional paid-in capital |
|
388,979 |
|
|
|
353,890 |
|
Accumulated other comprehensive income |
|
27 |
|
|
|
50 |
|
Accumulated deficit |
|
(101,400 |
) |
|
|
(39,367 |
) |
Total stockholders’ equity |
|
287,618 |
|
|
|
314,585 |
|
Total liabilities and stockholders’ equity |
$ |
325,558 |
|
|
$ |
375,225 |
|
OMNIAB, INC. |
|||||||||||||||
CONSOLIDATED STATEMENTS OF OPERATIONS |
|||||||||||||||
(unaudited, in thousands, except per share data) |
|||||||||||||||
|
Three Months Ended December 31, |
|
Year Ended December 31, |
||||||||||||
|
2024 |
|
2023 |
|
2024 |
|
2023 |
||||||||
Revenue: |
|
|
|
|
|
|
|
||||||||
License and milestone revenue |
$ |
8,650 |
|
|
$ |
1,713 |
|
|
$ |
13,866 |
|
|
$ |
20,699 |
|
Service revenue |
|
2,533 |
|
|
|
2,755 |
|
|
|
11,949 |
|
|
|
12,180 |
|
Royalty revenue |
|
(379 |
) |
|
|
354 |
|
|
|
576 |
|
|
|
1,285 |
|
Total revenue |
|
10,804 |
|
|
|
4,822 |
|
|
|
26,391 |
|
|
|
34,164 |
|
Operating expenses: |
|
|
|
|
|
|
|
||||||||
Research and development |
|
13,306 |
|
|
|
14,766 |
|
|
|
55,110 |
|
|
|
56,525 |
|
General and administrative |
|
7,360 |
|
|
|
7,869 |
|
|
|
30,741 |
|
|
|
33,313 |
|
Amortization of intangibles |
|
6,059 |
|
|
|
3,407 |
|
|
|
17,407 |
|
|
|
13,554 |
|
Other operating (income) expense, net |
|
(41 |
) |
|
|
(14 |
) |
|
|
(2,365 |
) |
|
|
191 |
|
Total operating expenses |
|
26,684 |
|
|
|
26,028 |
|
|
|
100,893 |
|
|
|
103,583 |
|
Loss from operations |
|
(15,880 |
) |
|
|
(21,206 |
) |
|
|
(74,502 |
) |
|
|
(69,419 |
) |
Other income (expense), net: |
|
|
|
|
|
|
|
||||||||
Interest income |
|
655 |
|
|
|
1,181 |
|
|
|
3,106 |
|
|
|
5,055 |
|
Other income (expense), net |
|
2 |
|
|
|
(3 |
) |
|
|
(15 |
) |
|
|
1 |
|
Total other income (expense), net |
|
657 |
|
|
|
1,178 |
|
|
|
3,091 |
|
|
|
5,056 |
|
Loss before income taxes |
|
(15,223 |
) |
|
|
(20,028 |
) |
|
|
(71,411 |
) |
|
|
(64,363 |
) |
Income tax benefit |
|
2,155 |
|
|
|
5,975 |
|
|
|
9,378 |
|
|
|
13,744 |
|
Net loss |
$ |
(13,068 |
) |
|
$ |
(14,053 |
) |
|
$ |
(62,033 |
) |
|
$ |
(50,619 |
) |
|
|
|
|
|
|
|
|
||||||||
Net loss per share, basic and diluted |
$ |
(0.12 |
) |
|
$ |
(0.14 |
) |
|
$ |
(0.61 |
) |
|
$ |
(0.51 |
) |
Weighted-average shares outstanding, basic and diluted |
|
104,795 |
|
|
|
100,162 |
|
|
|
102,365 |
|
|
|
99,683 |
|
View source version on businesswire.com: https://www.businesswire.com/news/home/20250318636844/en/
OmniAb, Inc.
Neha Singh, Ph.D.
investors@OmniAb.com
X @OmniAbTech
(510) 768-7760
Source: OmniAb, Inc.