Evofem Reports Financial Results for Third Quarter of 2025, Provides Business Update
Evofem (OTCID: EVFM) reported Q3 2025 results: net sales $5.0M (up 10% vs. prior-year quarter) and operating income $1.0M versus a $2.4M operating loss a year earlier. Total operating expenses fell to $4.0M, a 42% decline driven by a $1.0M decrease in G&A and a $1.9M one-time accounting gain tied to an expired Rush patent contingent royalty.
The company reported a net loss attributable to common stockholders of $1.7M (loss per share $0.01) vs. $2.4M ($0.02) in Q3 2024. Liquidity included $0.8M restricted cash at September 30, 2025. Corporate and commercial updates: submitted SOLOSEC for UAE approval, ongoing NIH-funded Phase 4 trial for SOLOSEC vs metronidazole, terminated the proposed merger with Aditxt, and advanced manufacturing cost reductions of ~50% for PHEXX and SOLOSEC.
Evofem (OTCID: EVFM) ha riportato i risultati del terzo trimestre 2025: vendite nette 5,0 milioni di dollari (in aumento del 10% rispetto al trimestre dell'anno precedente) e utile operativo 1,0 milioni di dollari contro una perdita operativa di 2,4 milioni di dollari un anno prima. Le spese operative totali sono diminuite a 4,0 milioni di dollari, un calo del 42% guidato da una diminuzione di 1,0 milioni di dollari nelle spese generali e amministrative e da un guadagno contabile una tantum di 1,9 milioni di dollari legato a una royalty contingente per un vecchio brevetto Rush scaduto.
L'azienda ha riportato una perdita netta attribuibile agli azionisti ordinari di 1,7 milioni di dollari (perdita per azione 0,01 $) rispetto ai 2,4 milioni ($0,02) del Q3 2024. La liquidità includeva contanti restricti di 0,8 milioni di dollari al 30 settembre 2025. Aggiornamenti societari e commerciali: presentata la domanda per SOLOSEC per l'approvazione negli UAE, trial di fase 4 finanziato dal NIH in corso per SOLOSEC vs metronidazolo, terminata la fusione proposta con Aditxt e avanzate riduzioni dei costi di produzione di circa 50% per PHEXX e SOLOSEC.
Evofem (OTCID: EVFM) reportó resultados del 3T 2025: ventas netas de 5,0 millones de dólares (un aumento del 10% frente al trimestre del año anterior) y ingreso operativo de 1,0 millones de dólares frente a una pérdida operativa de 2,4 millones de dólares un año antes. Los gastos operativos totales cayeron a 4,0 millones de dólares, una disminución del 42% impulsada por una reducción de 1,0 millones de dólares en gastos generales y administrativos y una ganancia contable puntual de 1,9 millones de dólares vinculada a una regalía contingente por una patente Rush vencida.
La empresa reportó una pérdida neta atribuible a accionistas comunes de 1,7 millones de dólares (pérdida por acción 0,01) frente a 2,4 millones de dólares (0,02) en el Q3 2024. La liquidez incluía efectivo restringido de 0,8 millones de dólares al 30 de septiembre de 2025. Actualizaciones corporativas y comerciales: se presentó SOLOSEC para aprobación en los UAE, ensayo de fase 4 financiado por NIH en curso para SOLOSEC vs metronidazol, terminada la fusión propuesta con Aditxt y se avanzaron reducciones de costos de fabricación de ~50% para PHEXX y SOLOSEC.
Evofem (OTCID: EVFM)은 2025년 3분기 실적을 발표했습니다: 순매출 500만 달러 (전년 동기 대비 10% 증가) 및 영업이익 100만 달러, 1년 전 240만 달러의 영업손실과 대조적입니다. 총 영업비용은 400만 달러로 감소했고, 이는 G&A 비용이 100만 달러 감소하고 만료된 Rush 특허에 따른 현금성 로열티와 관련된 일회성 회계상 이익 190만 달러가 반영된 결과입니다.
회사는 보통주주 귀속 순손실 170만 달러를 보고했습니다(주당 손실 0.01달러) 2024년 3분기 240만 달러(0.02달러) 대비. 유동성은 2025년 9월 30일 현재 제한 현금 80만 달러를 포함합니다. 기업 및 상업 업데이트: UAE 승인을 위한 SOLOSEC 제출, SOLOSEC 대 메트로니다졸 비교를 위한 NIH‑펀드 Phase 4 임상 진행 중, Aditxt와의 인수합병 제안 종료, PHEXX 및 SOLOSEC의 제조원가 약 50% 감소 추진.
Evofem (OTCID: EVFM) a publié les résultats du T3 2025: ventes nettes de 5,0 millions de dollars (-en hausse de 10% par rapport au trimestre correspondant de l'année précédente) et résultat opérationnel de 1,0 million de dollars contre une perte opérationnelle de 2,4 millions de dollars l'année précédente. Les coûts opérationnels totaux ont diminué à 4,0 millions de dollars, soit une baisse de 42% tirée par une diminution de 1,0 million de dollars des frais généraux et administratifs et un gain comptable ponctuel de 1,9 million de dollars lié à une redevance contingente pour un brevet Rush expiré.
La société a enregistré une perte nette attribuable aux actionnaires ordinaires de 1,7 million de dollars (perte par action 0,01$) contre 2,4 millions ($0,02) au T3 2024. La liquidité comprenait 80 000 $ en espèces restreints au 30 septembre 2025. Mises à jour corporatives et commerciales: soumission de SOLOSEC pour approbation aux ÉAU, essai de phase 4 financé par le NIH en cours pour SOLOSEC vs métronidazole, termination de la fusion proposée avec Aditxt et réduction des coûts de fabrication d'environ 50% pour PHEXX et SOLOSEC.
Evofem (OTCID: EVFM) hat die Ergebnisse des dritten Quartals 2025 vorgelegt: Nettoverkäufe 5,0 Mio. $ (gegenüber dem Vorjahresquartal um 10% gestiegen) und operativer Gewinn 1,0 Mio. $ gegenüber einem OPERATIVEN VERLUST von 2,4 Mio. $ im Vorjahr. Die gesamten Betriebskosten sanken auf 4,0 Mio. $, ein Rückgang von 42%, angetrieben durch eine Reduktion der G&A um 1,0 Mio. $ und einen einmaligen bilanzrechtlichen Gewinn von 1,9 Mio. $ im Zusammenhang mit einer ausgelaufenen Rush-Patent-Contingent-Royalty.
Das Unternehmen meldete einen netto Verlust, der den Aktionären der Stammaktien zuzurechnen ist, von 1,7 Mio. $ (Verlust pro Aktie 0,01 $) gegenüber 2,4 Mio. $ (0,02 $) im Q3 2024. Die Liquidität umfasste eingeschränktes Bargeld von 0,8 Mio. $ zum 30. September 2025. Unternehmens- und kommerzielle Updates: Einreichung von SOLOSEC für die Zulassung in den VAE, NIH-finanziierte Phase-4-Studie zu SOLOSEC vs Metronidazol, Beendigung der vorgeschlagenen Fusion mit Aditxt und Reduzierung der Herstellungskosten um ca. 50% für PHEXX und SOLOSEC.
Evofem (OTCID: EVFM) أبلغت عن نتائج الربع الثالث من 2025: المبيعات الصافية 5.0 مليون دولار (ارتفاع بنسبة 10% مقارنة بالربع نفسه من العام السابق) والدخل التشغيلي 1.0 مليون دولار مقابل فقدان تشغيلي 2.4 مليون دولار في العام السابق. انخفضت إجمالي المصروفات التشغيلية إلى 4.0 ملايين دولار، بانخفاض 42% مدفوعاً بانخفاض 1.0 مليون دولار في المصروفات العامة والإدارية وارتفاع فريد بمقدار 1.9 مليون دولار نتيجة ربح محاسبي مؤقت مرتبط بحق امتياز contingent يتعلق ببراءة Rush المنتهية.
أفادت الشركة بخسارة صافية تخص أصحاب الأسهم العادية بمقدار 1.7 مليون دولار (خسارة للسهم 0.01$) مقابل 2.4 مليون دولار (0.02) في الربع الثالث من 2024. شملت السيولة نقدًا مقيدًا قدره 0.8 مليون دولار في 30 سبتمبر 2025. تحديثات الشركات والعمليات: تقديم SOLOSEC للموافقة في الإمارات، تجربة المرحلة الرابعة الممولة من NIH قيد التنفيذ لـ SOLOSEC مقابل المترونيدازول، إنهاء الاندماج المقترح مع Aditxt، وتقدم في خفض تكاليف التصنيع بنحو 50% لـ PHEXX وSOLOSEC.
- Net sales increased by 10% to $5.0 million in Q3 2025
- Reported $1.0 million operating income in Q3 2025
- Operating expenses down to $4.0 million (42% reduction)
- Advanced ~50% manufacturing cost reduction strategies for PHEXX and SOLOSEC
- SOLOSEC submitted for marketing approval in the United Arab Emirates
- Net loss attributable to common stockholders of $1.7 million in Q3 2025
- Restricted cash was only $0.8 million as of September 30, 2025
- Stockholders did not approve merger with Aditxt; Merger Agreement terminated
-- Increased Net Sales
-- Delivered
"Sales rebounded in the third quarter and were
Notable developments since July 1st include:
- Increased net sales to
in the third quarter of 2025 compared to$5.0 million in the prior year quarter.$4.5 million - Posted operating income of
, compared to a loss from operations of$1.0 million in the prior year quarter.$2.4 million - Advanced strategies to reduce manufacturing costs by approximately
50% for both PHEXX® (lactic acid, citric acid and potassium bitartrate) and SOLOSEC® (secnidazole) 2g oral granules. In addition to increasing per-unit profit, the lower COGS are expected to facilitate entry into price-sensitive global markets for both products. -
SOLOSEC® was submitted for marketing approval in the
United Arab Emirates in the third quarter of 2025 under our June 2025 License and Supply Agreement with Pharma 1. - Patient recruitment is ongoing in an investigator-led, NIH-funded Phase 4 clinical trial evaluating the effectiveness and cost-effectiveness of SOLOSEC® (single-dose, one time) versus metronidazole (twice daily for seven days) for the treatment of Trichomonas vaginalis in men and women. Study investigators hypothesize that the rate of repeat infections with T. vaginalis will be 1.75 lower in the SOLOSEC group versus the multi-dose oral metronidazole arm and that single-dose SOLOSEC will have higher initial cost but will be more cost effective compared to multi-dose metronidazole, largely due to lower breakthrough rates of infection. 1
- Following the Special Meeting of Stockholders on October 20, 2025 at which Evofem's stockholders did not approve the merger transaction with Aditxt, Evofem exercised its rights to terminate the Merger Agreement.
Third Quarter Financial Results
For the three months ended September 30, 2025, net sales were
Total operating expenses decreased to
As a result, Evofem reported
Net loss attributable to common stockholders was
Liquidity
The Company had restricted cash of
About Evofem
Evofem Biosciences is commercializing innovative products to address unmet needs in women's sexual and reproductive health. The Company generates revenue from the sale of two FDA-approved products.
- PHEXX® (lactic acid, citric acid, and potassium bitartrate) is the first and only hormone-free, on-demand prescription contraceptive vaginal gel. It comes in a box of 12 pre-filled applicators and is applied 0-60 minutes before each act of sex. Visit phexxi.com to learn more and for important safety information.
- SOLOSEC® (secnidazole) 2 g oral granules is an FDA-approved oral antibiotic for the treatment of two sexual health diseases: bacterial vaginosis (BV), a common vaginal infection, in females 12 years of age and older, and trichomoniasis, a common sexually transmitted infection (STI), in people 12 years of age and older. SOLOSEC provides a complete course of therapy in just one dose. Visit solosec.com to learn more and for important safety information.
PHEXX®, PHEXXI® and SOLOSEC® are registered trademarks of Evofem Biosciences, Inc.
Sources
- National Institute of Allergy & Infectious Diseases (NIAID) of the National Institutes of Health. Award number R01AI183266: Refining Trichomonas vaginalis treatment in women and men.
Forward-Looking Statements
This press release includes "forward-looking statements," within the meaning of the safe harbor for forward-looking statements provided by Section 21E of the Securities Exchange Act of 1934, as amended, and the Private Securities Litigation Reform Act of 1995. Words such as, but not limited to, "anticipate," "aim," "believe," "contemplate," "continue," "could," "design," "estimate," "expect," "intend," "may," "might," "plan," "possible," "potential," "predict," "project," "seek," "should," "suggest," "strategy," "target," "will," "would," and similar expressions or phrases, or the negative of those expressions or phrases, are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. These statements include but are not limited to Evofem's expectations regarding the anticipated impact of COGS reduction initiatives, future sales trends, cost-reduction initiatives, manufacturing efficiencies, international market expansion, and the Company's ability to obtain additional financing or other strategic alternatives. Forward-looking statements are based on current assumptions and involve known and unknown risks and uncertainties, many of which are beyond the Company's control. Important factors that could cause actual results to differ materially from those discussed or implied in the forward-looking statements include, but are not limited to, limited cash resources, dependence on new capital or business development transactions to fund operations, potential delays in regulatory approvals, changes in market demand, manufacturing and supply chain risks, the nonrecurring nature of certain recent gains, together with those that are disclosed in the Company's SEC filings, including its Annual Report on Form 10-K for the year ended December 31, 2024 filed with the SEC on March 24, 2025, amended on March 28, 2025, Quarterly Report on Form 10-Q for the quarter ended September 30, 2025, filed with the SEC on November 13, 2025, and any subsequent filings. All forward-looking statements are expressly qualified in their entirety by such factors. Evofem undertakes no obligation to update or revise any forward-looking statement except as required by law, and investors are cautioned not to place undue reliance on such statements given the Company's current liquidity position and evolving business conditions.
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Investors and Potential Partners
Amy Raskopf, Chief Business Development Officer
Evofem Biosciences, Inc.
araskopf@evofem.com
(917) 673-5775
Financial tables follow
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EVOFEM BIOSCIENCES, INC., AND SUBSIDIARIES |
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CONDENSED CONSOLIDATED BALANCE SHEETS |
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(unaudited) |
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(In thousands) |
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As of |
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September 30, 2025 |
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December 31, 2024 |
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Cash and cash equivalents |
$ - |
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$ - |
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Restricted cash |
$ 840 |
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$ 741 |
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Trade accounts receivable, net |
$ 4,435 |
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$ 9,832 |
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Total current liabilities |
$ 78,186 |
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$ 80,448 |
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Total stockholders' deficit |
$ (75,066) |
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$ (71,257) |
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Total liabilities, convertible and redeemable preferred |
$ 13,807 |
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$ 23,789 |
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EVOFEM BIOSCIENCES, INC., AND SUBSIDIARIES |
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CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS |
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(unaudited) |
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(In thousands, except share and per share data) |
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Three Months Ended |
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Nine Months Ended |
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2025 |
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2024 |
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2025 |
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2024 |
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Product sales, net |
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$ 4,952 |
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$ 4,496 |
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$ 10,622 |
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$ 12,259 |
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Operating Expenses: |
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Cost of goods sold |
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905 |
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869 |
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2,025 |
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2,322 |
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Gain on change in accounting estimates |
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(1,933) |
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- |
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(1,933) |
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- |
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Amortization of intangible asset |
|
80 |
|
301 |
|
410 |
|
301 |
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Research and development, net |
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470 |
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332 |
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(3,819) |
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1,196 |
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Selling and marketing |
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2,391 |
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2,382 |
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7,616 |
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6,970 |
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General and administrative |
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2,088 |
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3,052 |
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6,296 |
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8,143 |
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Total operating expenses |
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4,001 |
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6,936 |
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10,595 |
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18,932 |
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Income (loss) from operations |
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951 |
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(2,440) |
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27 |
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(6,673) |
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Other income (expense): |
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Interest income |
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3 |
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3 |
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13 |
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13 |
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Other expense, net |
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(682) |
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(562) |
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(1,944) |
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(1,736) |
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Loss on issuance of financial instruments |
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- |
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- |
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- |
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(3,300) |
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Gain (loss) on debt extinguishment, net |
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- |
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(143) |
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- |
|
977 |
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Change in fair value of financial |
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(1,845) |
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769 |
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(490) |
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4,896 |
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Total other income (expense), net |
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(2,524) |
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67 |
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(2,421) |
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850 |
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Loss before income tax |
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(1,573) |
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(2,373) |
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(2,394) |
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(5,823) |
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Income tax benefit (expense) |
|
4 |
|
8 |
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(3) |
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- |
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Net loss |
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(1,569) |
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(2,365) |
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(2,397) |
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(5,823) |
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Convertible and redeemable preferred stock |
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(111) |
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(5) |
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(115) |
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(99) |
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Net loss attributable to common stockholders |
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$ (1,680) |
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$ (2,370) |
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$ (2,512) |
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$ (5,922) |
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Net loss per share attributable to common |
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$ (0.01) |
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$ (0.02) |
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$ (0.02) |
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$ (0.09) |
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Weighted-average shares used to compute net |
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119,578,093 |
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96,459,121 |
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116,229,614 |
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64,924,454 |
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SOURCE Evofem Biosciences, Inc.