Eiger BioPharmaceuticals, Inc.

OTCPK:EIGR.Q 주식 리포트

시가총액: US$12.6m

This company is no longer active

The company may no longer be operating, as it may be out of business. Find out why through their latest events.

Eiger BioPharmaceuticals 경영진

경영진 기준 점검 1/4

Eiger BioPharmaceuticals CEO는 David Apelian, Dec2022 에 임명되었습니다 의 임기는 1.83 년입니다. 총 연간 보상은 $1.48M, 42.3% 급여 및 57.7% 보너스(회사 주식 및 옵션 포함)로 구성됩니다. 는 $263.77K 가치에 해당하는 회사 주식의 2.1% 직접 소유합니다. 경영진과 이사회의 평균 재임 기간은 1.7 년과 6.3 년입니다.

핵심 정보

David Apelian

최고경영자

US$1.5m

총 보수

CEO 급여 비율42.31%
CEO 재임 기간1.8yrs
CEO 지분 보유율2.1%
경영진 평균 재임 기간1.7yrs
이사회 평균 재임 기간6.3yrs

최근 경영진 업데이트

Recent updates

분석 기사 Apr 01

Eiger BioPharmaceuticals, Inc.'s (NASDAQ:EIGR) 28% Dip In Price Shows Sentiment Is Matching Revenues

Eiger BioPharmaceuticals, Inc. ( NASDAQ:EIGR ) shareholders that were waiting for something to happen have been dealt a...
분석 기사 Jan 04

The Market Doesn't Like What It Sees From Eiger BioPharmaceuticals, Inc.'s (NASDAQ:EIGR) Revenues Yet As Shares Tumble 26%

Eiger BioPharmaceuticals, Inc. ( NASDAQ:EIGR ) shareholders won't be pleased to see that the share price has had a very...
분석 기사 Dec 20

Analysts Have Just Cut Their Eiger BioPharmaceuticals, Inc. (NASDAQ:EIGR) Revenue Estimates By 22%

The latest analyst coverage could presage a bad day for Eiger BioPharmaceuticals, Inc. ( NASDAQ:EIGR ), with the...
분석 기사 Nov 09

Analyst Forecasts For Eiger BioPharmaceuticals, Inc. (NASDAQ:EIGR) Are Surging Higher

Shareholders in Eiger BioPharmaceuticals, Inc. ( NASDAQ:EIGR ) may be thrilled to learn that the analysts have just...
분석 기사 Oct 06

Rock star Growth Puts Eiger BioPharmaceuticals (NASDAQ:EIGR) In A Position To Use Debt

Warren Buffett famously said, 'Volatility is far from synonymous with risk.' So it seems the smart money knows that...
Seeking Alpha Oct 05

Eiger sheds ~20% on abandonment of EUA request for COVID therapy

Eiger BioPharmaceuticals, Inc. (NASDAQ:EIGR), a biotech focused on rare and ultra-rare diseases, slipped ~20% pre-market Wednesday after announcing it would not seek an emergency use authorization (EUA) application in the U.S. for COVID-19 therapy peginterferon lambda. The decision followed a pre-EUA meeting the company had requested from the FDA. The agency denied the request citing issues in an investigator-sponsored trial designed to assess different therapeutic agents, including peginterferon, in non-hospitalized patients with mild-to-moderate COVID-19. FDA has determined that “any authorization request based on these data is unlikely to meet the statutory criteria for issuance of an EUA in the current context of the pandemic,” the company said. Instead, the agency has suggested that EIGR consider requesting an end-of-Phase 2 meeting to run a company-sponsored pivotal trial targeted at a Biologics License Application (BLA). EIGR is weighing the next steps, including strategic options to advance peginterferon lambda against respiratory viral agents, including COVID-19. Read: In September, the FDA updated its COVID-19 test policy to cut the number of reviews of EUA requests for diagnostic tests.
Seeking Alpha Sep 06

Eiger falls 21% amid uncertainty over regulatory path for COVID-19 therapy

The shares of commercial-stage biotech Eiger BioPharmaceuticals, Inc. (NASDAQ:EIGR) fell ~21% in the pre-market Tuesday after the company announced that the FDA is uncertain about the regulatory path for COVID-19 therapy peginterferon lambda. The update comes after the company's meeting with the regulator regarding the Phase 3 TOGETHER study for peginterferon lambda aimed at its emergency use authorization (EUA). Following the meeting, the FDA has indicated its uncertainty if the company can meet the requirements for a EUA submission for peginterferon lambda. However, EIGR remains in talks with the FDA as the regulator indicated its intention to consider any new data from the TOGETHER trial to support a EUA while the company plans to further develop the candidate in COVID-19.
Seeking Alpha Jul 26

Eiger BioPharmaceuticals: Undervalued Biotech With End Of 2022 Catalyst

European Commission granted marketing authorization for Zokinvy (lonafarnib) for the treatment of patients with progeria on July 20, 2022. Results from the phase 3 D-LIVR study using Lonafarnib for the treatment of patients with Hepatitis Delta Virus are expected by end of 2022. In March of 2022, a single dose of peginterferon Lambda for Covid-19, reduced the risk of hospitalization or ER visits greater than 6 hours by 50% in a predominantly vaccinated population. An Emergency Use Authorization filing from Eiger BioPharmaceuticals to the FDA for peginterferon Lambda for Covid-19 is possible in 2022. Eiger BioPharmaceuticals (EIGR) is a great speculative biotech play to look into. That's because it has a major catalyst for investors to look forward to at the end of 2022. This would be the readout of the phase 3 D-LIVR study, which is using Lonafarnib for the treatment of patients with Hepatitis Delta Virus ((HDV)). There is potential here to eventually possibly obtain approval for two combinations. These combinations include Lonafarnib and ritonavir and in combination with peginterferon alfa. In addition, this biotech had already received European approval for its treatment Zokinvy (Lonafarnib) for the treatment of patients with progeria. It is the first and only treatment approved in Europe for this specific indication. In addition, another possible catalyst would be Emergency Use Authorization (EUA) for Peginterferon Lambda for Covid-19 infection. The company is engaging with the FDA and intends to submit an EUA application along with the full set of results from the TOGETHER study. It was done in a predominantly vaccinated patient population, so it remains to be seen how well it does if it is ultimately approved. Regardless, I believe EUA could act as a trade opportunity. These are the reasons why I believe that Eiger BioPharmaceuticals is a great speculative biotech play to look into. Lonafarnib Catalyst Expected End Of 2022 Lonafarnib is in clinical development for the treatment of patients with Hepatitis Delta Virus. Hepatitis Delta Virus ((HDV)) or Hepatitis D is a very small circular RNA virus. It is one of the smallest types of virus that infects humans. However, right off the bat I will tell you that it is rare. Why is it rare? That's because in order for the HDV to infect someone, they also have to be carrying Hepatitis B (HBV). That's right, HDV needs HBV in order to infect a person. That's the only way HDV can replicate in liver cells. Those who may be at risk of getting HDV are those who have gone through many blood transfusions and those who are intravenous types of drug abusers. Symptoms of those who have this virus are as follows: Abdominal type pain Nausea Fatigue Being rare, there are roughly only about less than 200,000 people in the United States who have it. Eiger estimates that an HDV product could be about a >$1 billion per year market opportunity. The good news is that this program is already ongoing and still enrolling patients. This is known as the phase 3 D-LIVR study, which is estimated to enroll about 400 patients total. At least 300 patients will be treated with Lonafarnib. There are going to be two arms in the study as follows: All oral arm of LNF (lonafarnib) boosted with RTV (ritonavir) LNF boosted with RTV combined with pegylated interferon-alfa (PEG IFN-alfa) Each of the 2 arms above are going to be compared to placebo. That means in order for this study to be successful, it just needs to meet the primary endpoint compared to placebo. The composite primary endpoint is twofold as follows: Compare composite virologic and biochemical response rate at end of treatment ((EOT)) in patients who receive 50 mg Lonafarnib/100 mg BID Ritonavir versus patients who receive placebo (over 48 weeks) Compare composite virologic and biochemical response rate at end of EOT in patients who receive 50 mg Lonafarnib/100 mg BID Ritonavir and 180 mcg QW PEG IFN-alfa-2a (over 48 weeks)
Seeking Alpha Jul 20

European Commission approves Eiger BioPharmaceuticals' progeria therapy Zokinvy

Eiger BioPharmaceuticals (NASDAQ:EIGR) on Wednesday said the European Commission had granted a marketing authorization to its treatment Zokinvy (lonafarnib) for progeria, which is a progressive genetic disorder that causes accelerated aging. The specific indication for which Zokinvy was approved was as a breakthrough therapy in children and young adults with Hutchinson-Gilford progeria syndrome and processing-deficient progeroid laminopathies. The European approval for Zokinvy is valid in all 27 EU member states as well as Iceland, Liechtenstein and Norway. EIGR says Zokinvy is the first and only treatment approved in Europe for progeria. The therapy was approved by the U.S. FDA in 2020. EIGR stock +2.8% to $8.73 in early trading.

CEO 보수 분석

David Apelian의 보수는 Eiger BioPharmaceuticals의 수익에 비해 어떻게 변했나요?
날짜총 보수급여회사 수익
Dec 31 2023US$1mUS$626k

-US$75m

Sep 30 2023n/an/a

-US$87m

Jun 30 2023n/an/a

-US$96m

Mar 31 2023n/an/a

-US$97m

Dec 31 2022US$204kUS$31k

-US$97m

Sep 30 2022n/an/a

-US$93m

Jun 30 2022n/an/a

-US$89m

Mar 31 2022n/an/a

-US$86m

Dec 31 2021US$149kn/a

-US$34m

Sep 30 2021n/an/a

-US$31m

Jun 30 2021n/an/a

-US$24m

Mar 31 2021n/an/a

-US$21m

Dec 31 2020US$102kn/a

-US$65m

Sep 30 2020n/an/a

-US$63m

Jun 30 2020n/an/a

-US$66m

Mar 31 2020n/an/a

-US$68m

Dec 31 2019US$2mUS$272k

-US$70m

Sep 30 2019n/an/a

-US$70m

Jun 30 2019n/an/a

-US$68m

Mar 31 2019n/an/a

-US$61m

Dec 31 2018US$3mUS$514k

-US$52m

Sep 30 2018n/an/a

-US$47m

Jun 30 2018n/an/a

-US$39m

Mar 31 2018n/an/a

-US$40m

Dec 31 2017US$194kn/a

-US$42m

보상 대 시장: David의 총 보수(USD1.48M)는 US 시장에서 비슷한 규모 기업의 평균(USD630.36K)보다 높습니다.

보상과 수익: David의 보상은 회사가 적자임에도 증가했습니다.


CEO

David Apelian (59 yo)

1.8yrs
재임 기간
US$1,478,892
보수

Dr. David Apelian, M.D., Ph D., MBA, served as Chief Executive Officer and Director of Bluesphere Bio, Inc. since July 2019. Dr. Apelian served as Chief Operating Officer and Executive Medical Officer at E...


리더십 팀

이름직위재임 기간보수지분
David Apelian
CEO & Director1.8yrsUS$1.48m2.1%
$ 263.8k
James Vollins
General Counsel1.5yrsUS$548.12k0.27%
$ 34.0k
Christopher Kurtz
Chief Technical Officer2.5yrs데이터 없음데이터 없음
Douglas Staut
Chief Restructuring Officerless than a year데이터 없음데이터 없음
1.7yrs
평균 재임 기간
57yo
평균 나이

경험이 풍부한 관리: EIGR.Q의 경영진은 경험이 부족한 것으로 간주됩니다(평균 재임 1.7 년) — 신규 팀일 수 있습니다.


이사회 구성원

이름직위재임 기간보수지분
David Apelian
CEO & Director7.3yrsUS$1.48m2.1%
$ 263.8k
Thomas Dietz
Independent Chairman8.6yrsUS$170.00k0.36%
$ 45.6k
Amit Sachdev
Independent Director5.5yrsUS$67.50k0.099%
$ 12.5k
Lisa Kelly-Croswell
Independent Director2.3yrsUS$52.50k0%
$ 0
Stanley Rockson
Scientific Advisorno data데이터 없음데이터 없음
Evan Loh
Independent Director7.1yrsUS$69.50k0.099%
$ 12.5k
Tracey McLaughlin
Scientific Advisorno data데이터 없음데이터 없음
Kim Sablich
Director3.5yrsUS$57.00k0.077%
$ 9.6k
6.3yrs
평균 재임 기간
58yo
평균 나이

경험이 풍부한 이사회: EIGR.Q의 이사회경험이 있음으로 간주됩니다(평균 재임 6.3 년).


기업 분석 및 재무 데이터 상태

데이터최종 업데이트 (UTC 시간)
기업 분석2024/10/02 06:33
종가2024/10/01 00:00
수익2023/12/31
연간 수익2023/12/31

데이터 소스

당사의 기업 분석에 사용되는 데이터는 S&P Global Market Intelligence LLC에서 제공됩니다. 아래 데이터는 이 보고서를 생성하기 위해 분석 모델에서 사용됩니다. 데이터는 정규화되므로 소스가 제공된 후 지연이 발생할 수 있습니다.

패키지데이터기간미국 소스 예시 *
기업 재무제표10년
  • 손익계산서
  • 현금흐름표
  • 대차대조표
분석가 컨센서스 추정치+3년
  • 재무 예측
  • 분석가 목표주가
시장 가격30년
  • 주가
  • 배당, 분할 및 기타 조치
지분 구조10년
  • 주요 주주
  • 내부자 거래
경영진10년
  • 리더십 팀
  • 이사회
주요 개발10년
  • 회사 공시

* 미국 증권에 대한 예시이며, 비(非)미국 증권에는 해당 국가의 규제 서식 및 자료원을 사용합니다.

별도로 명시되지 않는 한 모든 재무 데이터는 연간 기간을 기준으로 하지만 분기별로 업데이트됩니다. 이를 TTM(최근 12개월) 또는 LTM(지난 12개월) 데이터라고 합니다. 자세히 알아보기.

분석 모델 및 스노우플레이크

이 보고서를 생성하는 데 사용된 분석 모델에 대한 자세한 내용은 당사의 Github 페이지에서 확인하실 수 있습니다. 또한 보고서 활용 방법에 대한 가이드YouTube 튜토리얼도 제공합니다.

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산업 및 섹터 지표

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분석가 소스

Eiger BioPharmaceuticals, Inc.는 11명의 분석가가 다루고 있습니다. 이 중 0명의 분석가가 우리 보고서에 입력 데이터로 사용되는 매출 또는 수익 추정치를 제출했습니다. 분석가의 제출 자료는 하루 종일 업데이트됩니다.

분석가기관
Madhu KumarBaird
Brian SkorneyBaird
Madhu KumarB. Riley Securities, Inc.