Immutep Limited

NasdaqGM:IMMP 주식 리포트

시가총액: US$63.1m

Immutep 대차대조표 건전성

재무 건전성 기준 점검 6/6

Immutep 의 총 주주 지분은 A$98.9M 이고 총 부채는 A$0.0, 이는 부채 대 자기자본 비율을 0% 로 가져옵니다. 총자산과 총부채는 각각 A$147.2M 및 A$48.3M 입니다.

핵심 정보

0%

부채/자본 비율

AU$0

부채

이자보상배율n/a
현금AU$99.13m
자본AU$98.90m
총부채AU$48.30m
총자산AU$147.20m

최근 재무 건전성 업데이트

업데이트 없음

Recent updates

Seeking Alpha • May 08

Immutep Limited: Surging On Positive Head And Neck Data

Summary Immutep's eftilagimod shows promising results in head and neck cancer, with a median overall survival of 17.6 months, significantly higher than what has been observed with other approaches. IMMP is well-capitalized with $146.3 million in liquidity, ensuring operations can continue without imminent dilution and funding issues. Despite promising phase 2 data, the fate of eftilagimod remains uncertain, with future trials and FDA discussions critical for potential accelerated approval. The positive TACTI-003 readout strengthens my "Buy" sentiment, though risks remain in this challenging cancer treatment landscape. Read the full article on Seeking Alpha
Seeking Alpha • Jan 28

Immutep Limited: Continuing To Make The Case For Eftilagimod

Summary Immutep Limited remains a “Buy” due to promising pipeline updates and strong financials, despite inherent high-risk/high-reward dynamics. Key trials for eftilagimod show encouraging results, particularly in non-small cell lung cancer and soft tissue sarcoma, enhancing the drug's potential. Financially, IMMP has a cash runway at least to 2026, supporting ongoing and future clinical trials without immediate funding concerns. Recent clinical data suggest meaningful advancements in LAG-3 therapeutics, reinforcing the investment thesis and highlighting IMMP's undervalued status. Read the full article on Seeking Alpha
Seeking Alpha • Nov 15

Immutep: Potential Of Efti As New Standard Of Care For NSCLC Patients

Summary Positive results from phase 1 INSIGHT-003 study, using eftilagimod alpha in combination with KEYTRUDA and chemotherapy in treating first-line metastatic non-squamous NSCLC patients. Additional data from the phase 1 INSIGHT-003 study is expected in 2025, with plans to initiate a phase 3 TACTI-004 study targeting the same patient population. The global non-small cell lung cancer market size is projected to reach $36.9 billion by 2031. Results from the phase 2b TACTI-003 study, using efti + KEYTRUDA to treat 1st-line recurrent/metastatic head and neck squamous cell carcinoma, expected in 2025; OS set as primary endpoint. Read the full article on Seeking Alpha
Seeking Alpha • Jul 15

Immutep: Positive Efti Treatment Data Leads To Late-Stage Programs

Summary Immutep Limited achieved positive results in the phase 2b study, using efti + Keytruda for the treatment of patients with 1st-line head and neck squamous cell carcinoma; Both PD-L1 positive and negative patients. Company to meet with FDA to be in a position to initiate a phase 3 study using efti + Keytruda for the treatment of patients with 1st-line HNSCC. Merck supply collaboration agreement in place to advance phase 3 study, using efti + Keytruda + chemotherapy for the treatment of 1stline NSCLC patients. Keytruda had become one of the top-selling drugs in 2023, with sales exceeding $25 billion; Efti has shown to help double several efficacy measures when added to Keytruda. Read the full article on Seeking Alpha
Seeking Alpha • May 01

Immutep: Realizing The Expected Catalysts, With More To Come

Summary Immutep Limited is focused on developing novel treatments targeting LAG3, an immune checkpoint, for various tumor types. The company's pipeline includes eftilagimod, which has shown promising response rates in thoracic malignancies. Immutep should have sufficient funding for 9–10 quarters of research and has demonstrated promising early signals of efficacy and safety. Read the full article on Seeking Alpha
Seeking Alpha • Oct 04

Immutep stock climbs on FDA fast track status for eftilagimod to treat lung cancer subtype

The U.S. Food and Drug Administration (FDA) granted fast track designation to Immutep's (NASDAQ:IMMP) eftilagimod alpha (IMP321) in combination with Merck's (NYSE:MRK) Keytruda (pembrolizumab) to treat first line non-small cell lung cancer (NSCLC). The combo was granted the status for initial treatment of patients with stage 3B/4 NSCLC expressing PD-L1 Tumor Proportion Score ≥1%, not amenable to EGFR/ALK based therapy, due to data from a phase 2 trial called TACTI-002/KEYNOTE-798, the company said in an Oct. 4 press release. "Efti also offers a chemotherapy-free option for NSCLC patients in need of less toxic and more durable solutions," said Immutep CEO Marc Voigt. The efti/Keytruda combo had previously received the FDA's fast track status in April 2021 as a first-line treatment for recurrent or metastatic Head and Neck Squamous Cell Carcinoma. IMMP +7.21% to $1.71 premarket Oct. 4
Seeking Alpha • Sep 23

Immutep secures €1.8M cash in French government's research tax credit

Immutep (NASDAQ:IMMP) announced Friday it has received €1.8M cash from the French government in research and development tax incentive payment. The incentive comes under the government's research tax credit scheme under which French companies conducting research and development activities in Europe can be reimbursed 30% of their eligible expenditure. The biotech firm said it intends to use the proceeds to support the ongoing and planned global clinical development of eftilagimod alpha and the preclinical development of IMP761. Stock is up 5% in pre-market trading. Earlier: Immutep gets Japanese patent for immunotherapy eftilagimod alpha combo
Seeking Alpha • Aug 30

Immutep gets Japanese patent for immunotherapy eftilagimod alpha combo

Immutep (NASDAQ:IMMP) said the Japanese Patent Office granted a new patent for eftilagimod alpha in combination with a PD-1 pathway inhibitor. The patent titled, 'Combined Preparations for the Treatment of Cancer or Infection' protects intellectual property related to combined therapeutic preparations consisting of  immunotherapy candidate eftilagimod alpha and an anti-PD-(L)1 antibody, the company said in an Aug. 30 press release. The company added that the claims are also directed to related methods of use in treating cancer and infection. "This is especially meaningful when coupled with the very promising data we have reported from TACTI-002 in three cancer indications, along with the initiation of TACTI-003 in the past 12 months," said Immutep CEO Marc Voigt. The patent is expected to expire Jan. 8, 2036.
Seeking Alpha • Jul 06

Immutep gets Japanese patent related to autoimmune disease drug candidate IMP761

Immutep (NASDAQ:IMMP) said it received a patent from the Japanese Patent Office related to its pre-clinical product candidate IMP761. The patent number number 7074341 titled 'Anti-LAG-3 Antibodies' is related to pharmaceutical compositions comprising IMP761 and the use of the compositions to treat T-cell mediated inflammatory and autoimmune diseases, according to the company's July 6 press release. The patent will expiry on Sept. 1, 2036.
Seeking Alpha • Jun 12

Immutep: Australian Immune-Focused Company, Pureplay LAG3 Player

Immutep has been developing anti-LAG3 compounds for over a decade. Recent approval of the first such compound from BMY was a watershed event. However, IMMP has a long way to go.
Seeking Alpha • Mar 21

Immutep - LAG3 Checkpoint Receives First FDA Approval; Positive For This LAG3 Pure Play

FDA approval of Bristol Myers Opdualag/relatlimab anti-LAG3 carries positive implications for LAG3 pure-play Immutep’s entire pipeline. From an anti-LAG3 perspective, the FDA approval is directly positive for Immutep's recently unveiled oral, small molecule anti-LAG3 program and its out-licensed anti-LAG3 program to Novartis. Like anti-PD1 (Keytruda, Opvido) & anti-CLTA4 (Yervoy), LAG3 may be a key checkpoint in oncology. Yet, unlike PD1/CTLA4, LAG3 is unique in that both its activation & inhibition kills cancer. This relatively unknown pure-play on the emerging checkpoint LAG3 (Lymphocyte Activating Gene-3) has collaborations with Novartis, Merck, Pfizer, Merck KGaA, GlaxoSmithKline, EOC Pharma, Labcorp, etc. As its clinical data continues to strengthen, like it consistently has over the past few years, Immutep is seemingly well situated for strategic deals or its potential acquisition.
Seeking Alpha • Jun 21

Immutep expands the evaluation of efti into a triple combination therapy, shares down 12%

Immutep (IMMP) has signed an agreement to commence a new Phase I trial, called INSIGHT-003, to evaluate the combination of lead product candidate eftilagimod alpha (“efti” or “IMP321”) in conjunction with an existing approved standard of care therapy consisting of a chemotherapy agent and an anti-PD-1 therapy. INSIGHT-003 will be run as an amendment to the protocol of the ongoing INSIGHT trial as the third arm (Stratum C) with Prof. Dr. Salah-Eddin Al-Batran as lead investigator. Up to 20 patients

재무 상태 분석

단기부채: IMMP 의 단기 자산 ( A$139.8M )이 단기 부채( A$47.0M ).

장기 부채: IMMP의 단기 자산(A$139.8M)이 장기 부채(A$1.3M)를 초과합니다.

부채/자본 비율 추이 및 분석

부채 수준: IMMP 부채가 없습니다.

부채 감소: IMMP는 5년 전 부채 대비 자본 비율이 15.6%였으나 현재 부채가 없습니다.

대차대조표

현금 보유 기간 분석

과거에 평균적으로 손실을 기록해 온 기업의 경우, 최소 1년 이상의 현금 보유 기간이 있는지 평가합니다.

안정적인 현금 활주로: IMMP 현재 무료 현금 흐름을 기준으로 1년 이상 충분한 현금 활주로를 보유하고 있습니다.

예측 현금 활주로: IMMP 26.5 1.7 26.5 % 매년.

건전한 기업 찾아보기

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기업 분석 및 재무 데이터 상태

데이터최종 업데이트 (UTC 시간)
기업 분석2026/05/25 10:24
종가2026/05/22 00:00
수익2025/12/31
연간 수익2025/06/30

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.

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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 가이드와 YouTube 튜토리얼도 제공합니다.

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산업 및 섹터 지표

산업 및 섹터 지표는 Simply Wall St가 6시간마다 계산하며, 프로세스에 대한 자세한 내용은 Github에서 확인할 수 있습니다.

분석가 소스

Immutep Limited는 14명의 분석가가 다루고 있습니다. 이 중 7명의 분석가가 우리 보고서에 입력 데이터로 사용되는 매출 또는 수익 추정치를 제출했습니다. 분석가의 제출 자료는 하루 종일 업데이트됩니다.

분석가기관
Melissa BensonBarrenjoey Markets Pty Limited
Thomas WakimBell Potter
Dylan DupuisB. Riley Securities, Inc.