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Article

A Novel Adaptable Weibull Distribution and Its Applications

by
Asmaa S. Al-Moisheer
1,
Khalaf S. Sultan
2,* and
Hossam M. M. Radwan
3
1
Department of Mathematics and Statistics, Faculty of Science, Imam Mohammad Ibn Saud Islamic University (IMSIU), Riyadh 11432, Saudi Arabia
2
Mathematics Department, Faculty of Science, Al-Azhar University, Nasr City, Cairo 11884, Egypt
3
Mathematics Department, Faculty of Science, Minia University, Minia 61519, Egypt
*
Author to whom correspondence should be addressed.
Axioms 2025, 14(7), 490; https://doi.org/10.3390/axioms14070490
Submission received: 24 May 2025 / Revised: 16 June 2025 / Accepted: 18 June 2025 / Published: 24 June 2025

Abstract

This work proposes a novel extension for a new extended Weibull distribution. Some statistical properties of the proposed distribution are studied including quantile, moments, skewness, and kurtosis. The hazard rate function of the new distribution has certain elastic qualities, allowing it to take increasing, upside-down bathtub, and modified upside-down bathtub shapes commonly observed in medical contexts. Different methods of estimation are studied using complete data. Two real data sets from the medical field are analyzed to demonstrate that the proposed model has adaptability in practice. In comparison to some well-known distributions, the suggested distribution fits the tested data better based on both parametric and non-parametric statistical criteria. A simulation study is presented to compare the obtained estimates based on mean square error and average absolute bias.

1. Introduction

The provided statistical lifetime distributions play a significant role in both the quality of the statistical analysis procedures and in the realization and forecasting of real-world phenomena. The statistician’s choice of model is made easier by the availability of many lifetime distributions that are available to them. Thus, the generalization of the existing lifetime distributions has become urgently necessary due to their flexibility because the data of many significant problems in engineering, medicine, and other areas are incompatible with or poorly fit by the available lifetime distributions. It is important and challenging to select the best statistical model for data analysis. As a result, several authors have worked very hard in recent years to propose new families that extend current distributions and offer adaptable classes for modeling data in many different areas.
In several disciplines, including medicine and reliability engineering, the Weibull distribution [1] is one of the most often utilized distributions. The complicated lifetime of some systems cannot be modeled by the Weibull distribution because it does not possess the property of bathtub-shaped or unimodal-shaped hazard rate functions. Several extensions to the Weibull distribution have been developed to address this issue.
Numerous publications, including [2,3,4,5,6], proposed several Weibull distribution extensions with more adaptable characteristics.
Additionally, the Weibull distribution also has two important extensions, namely, the modified Weibull distribution (MWD) [7] and new extended Weibull distribution (NEWD) [8], which are extremely significant in numerous applications. For the MWD’s HRF, only increasing or bathtub shapes are available, while the NEWD’s HRF only permits the use of increasing or upside-down bathtub shapes. Recently, many publications proposed several extension of distributions with HRFs with upside-down bathtub and modified upside-down bathtub shapes, including [9,10,11,12].
This study’s primary goal is to introduce a new extension known as the Modification for New Extended Weibull distribution, which has more flexible qualities than the New Extended Weibull distribution.
The following goals give a significant justification for the importance of the proposed distribution.
  • To present a novel lifetime distribution by extending the new extended Weibull distribution and discuss its advantages and potential uses.
  • To calculate the formula of the quantile in closed form and study the numerical results of the rth moment of the proposed distribution.
  • To show the hazard rate function of the new distribution can take not only the upside-down bathtub shape like NEWD but also the modified upside-down bathtub shape commonly observed in medical contexts.
  • To investigate several techniques of estimation for the new model’s unknown parameters based on complete data.
  • Using the ideas and techniques presented in this study, the significance of this new model in the medical field is demonstrated under complete data.
  • When applied to the clinical data, the new distribution demonstrates a superior fit compared to its sub-models and some well-known distributions.
  • The effectiveness of the various estimation strategies used to estimate the distribution parameters is investigated using a simulation study.
The article is divided into seven sections, each focusing on a particular topic of the study. In Section 2, the construction of the GNEWD is thoroughly detailed. In Section 3, some statistical properties are studied. The behavior of the HRF of the GNEWD is presented in Section 4. Section 5 is dedicated to studying the different techniques of estimation for the new model. Two applications are presented to demonstrate the practical relevance and effectiveness of the proposed methods based on real-life data in Section 6. A simulation study is carried out in Section 7 to evaluate the performance of the proposed estimators.

2. The New Modification for Weibull Distribution

The CDF of the GNEWD with parameter vector Θ = ( λ , γ , a , b ) is obtained by multiplying the cumulative hazard rate function for the Weibull distribution by the component e a x b
F ( x ; Θ ) = 1 e λ x γ e a x b , x > 0 ,
where λ > 0 is the scale parameter, and γ , a , b > 0 are the shape parameters.
Accordingly, the PDF, SF, and HRF of the GNEWD are given, respectively, as follows.
f ( x ; Θ ) = λ x γ 1 e λ x γ e a x b e a x b [ γ + a b x b ] , x > 0 ,
S ( x ; Θ ) = e λ x γ e a x b , x > 0 ,
and
h ( x ; Θ ) = λ x γ 1 e a x b [ γ + a b x b ] , x > 0 .
Some possible shapes for the PDF of the GNEWD are exhibited in Figure 1. Based on different values of parameters, the PDF of the GNEWD can be unimodal with a small and long right tail. Figure 2a exhibits the shapes for the CDF of the GNEWD and Figure 2b exhibits the shapes for the survival function of the GNEWD with different values of parameters of the GNEWD.
From Equation (1), some well-known distributions can be obtained as in Table 1.

3. Some Statistical Properties

In this section, an explicit form of the GNEWD’s quantile function is presented. This is required for generating random data samples from the proposed distribution to conduct the simulation study. It is also important to calculate the Bowley skewness and Moors kurtosis measures which are used to demonstrate a distribution’s asymmetry and tail behavior, respectively, utilizing quantile-based techniques that are less sensitive to outliers. Further, the formula for the moments of the GNEWD is studied.

3.1. Quantiles

Lemma 1. 
From (1), it is evident that the quantile function of the GNEWD can be given as follows:
x q = a b γ W a b log ( 1 q ) λ b γ γ 1 / b , 0 < q < 1 ,
where W . is the LambertW function [for more details, see [14]].
Proof 1. 
Let q = F ( x ; Θ ) ; then
q = 1 e λ x q γ e a x q b ,
by applying some algebraic calculation, we get
x q γ e a x q b = log ( 1 q ) λ ,
using the definition of the LambertW function, the result is satisfied. □
Let x q be the quantile of the GNEWD which is given by (5). Then the Bowley skewness and Moors kurtosis of the GNEWD can be given, respectively, as follows:
B S k e w = x 0.75 + x 0.25 2 x 0.5 x 0.75 x 0.25 ,
and
M k u r = x 0.875 x 0.625 + x 0.375 x 0.125 x 0.75 x 0.25 .

3.2. Moments

Moments are important in statistical analysis, both theoretically and practically. They provide crucial insights into probability distribution behavior by quantifying key properties like central tendency, variability, skewness, and kurtosis. Upon using (2), the rth moments of the GNEWD can be given as
μ r ( Θ ) = 0 x r λ x γ 1 e λ x γ e a x b e a x b [ γ + a b x b ] d x .
The integration in (8) cannot be calculated analytically. So, numerical method can be used to compute (8) using NIntegrate in Wolfram Mathematica 11.
The measurements of variance ( V a r ( Θ ) ) , skewness ( S k ( Θ ) ) , and kurtosis ( K u r ( Θ ) ) can be calculated, respectively, by using the first four ordinary moments of the GNEWD as:
V a r ( Θ ) = μ 2 ( Θ ) μ 1 ( Θ ) 2 ,
S k ( Θ ) = μ 3 ( Θ ) 3 μ 1 ( Θ ) μ 2 ( Θ ) + 2 μ 1 ( Θ ) 3 V a r ( Θ ) 3 / 2 ,
and
K u r ( Θ ) = μ 4 ( Θ ) 4 μ 1 ( Θ ) μ 3 ( Θ ) + 6 μ 1 ( Θ ) 2 μ 2 ( Θ ) 3 μ 1 ( Θ ) 4 V a r ( Θ ) 2 .
Some numerical values of the first four ordinary moments, variance, skewness, and kurtosis of the GNEWD are calculated and listed in Table 2. From Table 2, one can show that the following results are satisfied:
  • Under fixed values of ( λ , γ ) = ( 1 , 1 ) ,
    • As b increases with fixed a, the mean and variance of the GNEWD decrease.
    • As a increases with fixed b, the mean and variance of the GNEWD increase.
    • As b increases with fixed a, the skewness of the GNEWD decreases.
    • As a increases with fixed b, the skewness of the GNEWD decreases.
    • As b increases with fixed a, the kurtosis of the GNEWD increases.
    • As a increases with fixed b, the kurtosis of the GNEWD decreases.
  • Under fixed values of ( λ , γ ) = ( 3 , 3 ) ,
    • As b increases with fixed a, the mean of the GNEWD increases and variance of the GNEWD decreases.
    • As a increases with fixed b, the mean and variance of the GNEWD increase.
    • As b increases with fixed a, the skewness of the GNEWD decreases.
    • As a increases with fixed b, the skewness of the GNEWD decreases.
    • As b increases with fixed a, the kurtosis of the GNEWD increases.
    • As a increases with fixed b, the kurtosis of the GNEWD increases.

4. Some Attributes of the HRF

This section deals with some characterization of the HRF. The different shapes for the HRF of the GNEWD including increasing, upside-down bathtub, and modified upside-down bathtub shapes are shown in this section. From (4), one can show that the first derivative of h ( x ) can be written as
h ( x ; Θ ) = λ x γ 2 e a x b [ γ ( γ 1 ) + a b ( b + 2 γ 1 ) x b + a 2 b 2 x 2 b ] , x > 0 .
If b = 1 , Equation (12) reduces to
h ( x ; λ , γ , a ) = λ x γ 4 e a x [ γ ( γ 1 ) x 2 + 2 a ( γ 1 ) x + a 2 ] , x > 0
which is the same for NEWD as in [8].
Remark 1. 
For λ > 0 , b > 0 , and a > 0 , the following limits are satisfied:
1. 
lim x 0 + ( λ x γ 1 e a x b γ + a b x b ) 0 for 0 < γ < 1 .
2. 
lim x ( λ x γ 1 e a x b γ + a b x b ) 0 for 0 < γ < 1 .
3. 
lim x 0 + ( λ x γ 1 e a x b γ + a b x b ) 0 for γ = 1 .
4. 
lim x ( λ x γ 1 e a x b γ + a b x b ) λ for γ = 1 .
5. 
lim x 0 + ( λ x γ 1 e a x b γ + a b x b ) 0 for γ > 1 .
6. 
lim x ( λ x γ 1 e a x b γ + a b x b ) for γ > 1 .
It is easy to show that lim x 0 + h ( x ; Θ ) 0 for all values of γ > 0 using L’Hospital’s rule. Further, the value of the limit lim x h ( x ; Θ ) can be obtained directly as shown in Remark 1.
Lemma 2. 
For λ > 0 and a > 0 , the HRF take the following shapes:
  • h(x;Θ) has increasing shape from zero to infinity if γ > 1 and b 1 .
  • h(x;Θ) has increasing shape from 0 to λ if γ = 1 and b 1 .
  • h(x;Θ) has an upside-down bathtub shape if 0 < γ < 1 and b > 0 .
  • h(x;Θ) has a modified upside-down bathtub shape if 1 < γ 1 + 2 b + b 2 4 b and b > 1 .
Proof 2. 
Equation (12) can be rewritten as
h ( x ; Θ ) = λ x γ 2 b 2 e a x b [ γ ( γ 1 ) x 2 b + a b ( b + 2 γ 1 ) x b + a 2 b 2 ] .
Upon using (13) with the results in Remark 1, one can derived the following results:
  • For γ > 1 and b 1 , it is clear that h ( x ; Θ ) > 0 for all x > 0 . Then h ( x ; Θ ) has an increasing shape that goes from zero to as x .
  • For γ = 1 and b 1 , it is clear that h ( x ; Θ ) > 0 for all x > 0 . Then h ( x ; Θ ) has an increasing shape that goes from zero to λ as x .
  • For 0 < γ < 1 and b > 0 , it is clear that h ( x ; Θ ) has two roots based on the expression γ ( γ 1 ) x 2 + 2 a ( γ 1 ) x + a 2 which are given as follows: x 1 = a b ( b 2 γ + 1 ) a b b 2 4 b γ + 2 b + 1 2 γ ( γ 1 ) 1 / b and x 2 = a b ( b 2 γ + 1 ) + a b b 2 4 b γ + 2 b + 1 2 γ ( γ 1 ) 1 / b . Under the two conditions 0 < γ < 1 and b > 0 , it is evident that x 1 > 0 and x 2 < 0 because b 2 4 b γ + 2 b + 1 > ( b 2 γ + 1 ) . So, h ( x ; Θ ) has a unique root for x > 0 which is x 1 . Additionally, h ( x ; Θ ) > 0 when x < x 1 and h ( x ; Θ ) < 0 when x > x 1 . This means that the hazard rate function has an upside-down bathtub shape that converges to 0 when x approaches 0 or .
  • For 1 < γ 1 + 2 b + b 2 4 b and b > 1 , it is clear that h ( x ; Θ ) has two roots, x 1 and x 2 . Under the two conditions 1 < γ 1 + 2 b + b 2 4 b and b > 1 , it is clear that b 2 4 b γ + 2 b + 1 < ( b 2 γ + 1 ) , x 1 > 0 , x 2 > 0 , and x 2 > x 1 . So, there are two change points. Also, h ( x ; Θ ) > 0 when x < x 1 and x > x 2 and h ( x ; Θ ) < 0 when x > x 1 and x < x 2 (using R e d u c e in Wolfram Mathematica). This means that the hazard rate function has a modified upside-down bathtub shape.
Upon using different values of parameters as shown in the previous two lemmas, the behavior of the HRF of the GNEWD can be increasing, upside-down bathtub, and modified upside-down bathtub as shown in Figure 3.

5. Different Methods of Estimation

This section outlines five specific estimation techniques relevant to the GNEWD: MLE, LSE, WLSE, CVME, and ADE. These methods are utilized to estimate the unknown parameters of the new model.

5.1. Maximum Likelihood Estimation

Suppose that x 1 , , x n is an independent random sample of size n from the GNEWD. From Equation (2), the log-likelihood function can be obtained as
( Θ ) = n log ( λ ) i = 1 n λ x i γ e a x i b + i = 1 n log a b x i b + γ i = 1 n a x i b + ( γ 1 ) i = 1 n log x i .
By taking the first derivative ( Θ ( Θ ) = Θ ) of (14) with respect to λ , γ , a, and b we get
λ ( Θ ) = n λ i = 1 n x i γ e a x i b ,
γ ( Θ ) = i = 1 n log x i i = 1 n λ x i γ log x i e a x i b + i = 1 n 1 a b x i b + γ ,
a ( Θ ) = i = 1 n λ e a x i b x i γ b + i = 1 n b x i b a b x i b + γ i = 1 n x i b ,
and
b ( Θ ) = i = 1 n a λ log x i e a x i b x i γ b + i = 1 n a x i b a b x i b log x i a b x i b + γ i = 1 n a x i b log x i .

5.2. The Parameters λ , γ , a, and b Are Unknown

The MLE Θ ^ of Θ is given by solving the four normal equations λ ( Θ ) = 0 , γ ( Θ ) = 0 , a ( Θ ) = 0 , and b ( Θ ) = 0 . Since these equations cannot be solved analytically, they are solved numerically by employing F i n d R o o t in the Wolfram Mathematica 11 software. The initial values for the parameters can be obtained by fitting special GNEWD sub-models using F i n d D i s t r i b u t i o n P a r a m e t e r s in the Wolfram Mathematica 11 software.

5.3. Fisher Information Matrix

Since the computation of the Fisher information matrix (given by taking the expectation of the second derivative of (14)) is very difficult, it seems appropriate to approximate these expected values by their MLEs. Then, the asymptotic variance–covariance matrix is given as follows [see, [15]]:
V a r ( λ ^ ) C o v ( λ ^ , γ ^ ) C o v ( λ ^ , a ^ ) C o v ( λ ^ , b ^ ) C o v ( γ ^ , λ ^ ) V a r ( γ ^ ) C o v ( γ ^ , a ^ ) C o v ( γ ^ , b ^ ) C o v ( a ^ , λ ^ ) C o v ( a ^ , γ ^ ) V a r ( a ^ ) C o v ( b ^ , a ^ ) C o v ( b ^ , λ ^ ) C o v ( b ^ , γ ^ ) C o v ( b ^ , a ^ ) V a r ( b ^ ) = λ λ ( Θ ) λ γ ( Θ ) λ a ( Θ ) λ b ( Θ ) γ λ ( Θ ) γ γ ( Θ ) γ a ( Θ ) γ b ( Θ ) a λ ( Θ ) a γ ( Θ ) a a ( Θ ) a b ( Θ ) b λ ( Θ ) b γ ( Θ ) b a ( Θ ) b b ( Θ ) ( λ ^ , γ ^ , a ^ , b ^ ) 1 ,
where θ i θ j ( Θ ) = 2 θ i θ j , i , j = 1 , 2 , 3 , 4 , see Appendix A. Accordingly, the ACIs based on the asymptotic variance–covariance matrix for the parameters λ , γ , a, and b are, respectively, given as follows:
λ ^ ± z α 2 V a r ( λ ^ ) ,   γ ^ ± z α 2 V a r ( γ ^ ) ,   a ^ ± z α 2 V a r ( a ^ ) and   b ^ ± z α 2 V a r ( b ^ ) ,
where z α 2 is the percentile of the standard normal distribution with right tail probability α 2 . Even if the parameters are positive, the ACIs can yield a negative lower bound. In this case, the negative numbers could be substituted by zero.

5.4. Least Square and Weighted Least Square Estimations

The study [16] presents the LSE and WLSE for estimating the parameters of the beta distribution. These methods will estimate the parameters of the GNEWD. For this purpose, take x i , i = 1 , , n as the ordered sample of a random sample of size n. Then the LSE of the parameters of the GNEWD can be obtained by minimizing the following function:
S = i = 1 n F ( x i ; Θ ) i n + 1 2
with respect to the unknown parameters Θ or by solving the following non-linear equations:
S λ = i = 1 n 2 1 e λ x i γ e a x i b δ 1 ( x i ; Θ ) = 0 ,
S θ = i = 1 n 2 1 e λ x i γ e a x i b δ 2 ( x i ; Θ ) = 0 ,
S α = i = 1 n 2 1 e λ x i γ e a x i b δ 3 ( x i ; Θ ) = 0 ,
and
S γ = i = 1 n 2 1 e λ x i γ e a x i b δ 4 ( x i ; Θ ) = 0 ,
where
δ 1 ( x i ; Θ ) = x i γ e λ x i γ e a x i b a x i b ,
δ 2 ( x i ; Θ ) = λ x i γ log x i e λ x i γ e a x i b a x i b ,
δ 3 ( x i ; Θ ) = λ x i γ b e λ x i γ e a x i b a x i b ,
and
δ 4 ( x i ; Θ ) = a λ log x i x i γ b e λ x i γ e a x i b a x i b .
In order to determine the WLSE of the unknown parameters of the GNEWD, minimize the following function
W = i = 1 n ( n + 2 ) ( n + 1 ) 2 i ( n i + 1 ) F ( x i ; Θ ) i n + 1 2
with respect to the unknown parameters Θ or solve the non-linear equations
W λ = i = 1 n 2 ( n + 2 ) ( n + 1 ) 2 i ( n i + 1 ) 1 e λ x i γ e a x i b δ 1 ( x i ; Θ ) = 0 ,
W θ = i = 1 n 2 ( n + 2 ) ( n + 1 ) 2 i ( n i + 1 ) 1 e λ x i γ e a x i b δ 2 ( x i ; Θ ) = 0 ,
W α = i = 1 n 2 ( n + 2 ) ( n + 1 ) 2 i ( n i + 1 ) 1 e λ x i γ e a x i b δ 3 ( x i ; Θ ) = 0 ,
and
W γ = i = 1 n 2 ( n + 2 ) ( n + 1 ) 2 i ( n i + 1 ) 1 e λ x i γ e a x i b δ 4 ( x i ; Θ ) = 0 .
where δ 1 ( x i ; Θ ) , δ 2 ( x i ; Θ ) , δ 3 ( x i ; Θ ) , and δ 4 ( x i ; Θ ) are given by (16), (17), (18), and (19), respectively.

5.5. Cramér Von-Mises Estimation

In the study [17], it was shown that the bias of CVME is smaller than the other minimum distance estimator. The CVME of the GNEWD is obtained by minimizing the following function:
C = 1 12 r + i = 1 r F ( x i ; Θ ) 2 i 1 2 r 2
with respect to the unknown parameters Θ or by solving the following non-linear equations:
C λ = i = 1 r 2 1 e λ x i γ e a x i b δ 1 ( x i ; Θ ) = 0 ,
C θ = i = 1 r 2 1 e λ x i γ e a x i b δ 2 ( x i ; Θ ) = 0 ,
C α = i = 1 r 2 1 e λ x i γ e a x i b δ 3 ( x i ; Θ ) = 0 ,
and
C γ = i = 1 r 2 1 e λ x i γ e a x i b δ 4 ( x i ; Θ ) = 0 ,
where δ 1 ( x i ; Θ ) , δ 2 ( x i ; Θ ) , δ 3 ( x i ; Θ ) , and δ 4 ( x i ; Θ ) are given by (16), (17), (18), and (19), respectively.

5.6. Anderson Darling Estimation

Another study [18], studied the properties of ADE. From the results given there, the A-DE of the GNEWD is obtained by minimizing the following function:
A = r i = 1 r ( 2 i 1 ) r log F ( x i ; Θ ) + log ( 1 F ( x r i + 1 ; Θ ) ) ,
with respect to the unknown parameters Θ or by solving the following non-linear equations:
A λ = i = 1 r ( 2 i 1 ) r δ 1 ( x i ; Θ ) 1 e λ x i γ e a x i b δ 1 ( x r i + 1 ; Θ ) e λ x r i + 1 γ e a x r i + 1 b = 0 ,
A θ = i = 1 r ( 2 i 1 ) r δ 2 ( x i ; Θ ) 1 e λ x i γ e a x i b δ 2 ( x r i + 1 ; Θ ) e λ x r i + 1 γ e a x r i + 1 b = 0 ,
A α = i = 1 r ( 2 i 1 ) r δ 3 ( x i ; Θ ) 1 e λ x i γ e a x i b δ 3 ( x r i + 1 ; Θ ) e λ x r i + 1 γ e a x r i + 1 b = 0 ,
and
A γ = i = 1 r ( 2 i 1 ) r δ 4 ( x i ; Θ ) 1 e λ x i γ e a x i b δ 4 ( x r i + 1 ; Θ ) e λ x r i + 1 γ e a x r i + 1 b = 0 ,
where δ 1 ( x i ; Θ ) , δ 2 ( x i ; Θ ) , δ 3 ( x i ; Θ ) , and δ 4 ( x i ; Θ ) are given by (16), (17), (18), and (19), respectively.

6. Application to Real Data

In this section, three clinical real data sets are analyzed to show that the generalized new extended Weibull distribution (GNEWD) offers enhanced flexibility for modeling these data sets better than their sub-models and some well-known distributions. For every data set, the NGNEWD can be compared, using a non-parametric test like the Kolmogorov–Smirnov test (K-S) and parametric tests such as the Akaike information criterion (AIC) and Bayesian information criterion (BIC), with its sub models (NEWD, RGNEWD, RNEWD, and WD) and also with the following well-known distributions summarized in Table 3.

6.1. Liver Cancer Data

The data presented in [26], and analyzed in [27,28,29], includes records for 39 liver cancer patients. These patients were treated at Elminia Cancer Center, which operates under the Ministry of Health in Egypt. The cases were registered in the year 1999. The data set contains the lifetimes of the patients, measured in days, being 10, 14, 14, 14, 14, 14, 15, 17, 18, 20, 20, 20, 20, 20, 23, 23, 24, 26, 30, 30, 31, 40, 49, 51, 52, 60, 61, 67, 71, 74, 75, 87, 96, 105, 107, 107, 107, 116, 150.
For this data, Table 4 provides a summary of the numerical results of the parametric and non-parametric tests based on the MLEs of all comparison distributions. At a level of significance of α = 0.05 , it is possible to demonstrate that all distributions fit the liver cancer data based on the p-value related to the K-S test. Since the GNEWD has the lowest value based on the parametric tests AIC and BIC, it is clear from Table 4 that it fits this data better than other distributions. Based on the liver cancer data, Figure 4 displays the log-likelihood function profiles for each parameter. The approximate 95% CIs for λ , γ , a, and b are [0, 0.0439], [0, 296,323], [1.6289, 6.4285], and [0.6842, 1.4559], respectively, derived using the asymptotic variance–covariance matrix based on the MLEs for this data. Additionally, Table 5 provides the values of K-S along with the matching p-value for the liver cancer data, as well as all estimations of the unknown parameters based on the various approaches that were taken into consideration in an earlier section. Table 5 makes it clear that the ADE is the best approach for the liver cancer data when the K-S test is used with the associated p-value.

6.2. Plasma Concentrations of Indomethicin Data

Consider the following data set from [30] and analyzed by [31], which includes 66 observations of plasma concentrations of indomethicin (mcg/mL). The data are 1.50, 0.94, 0.78, 0.48, 0.37, 0.19, 0.12, 0.11, 0.08, 0.07, 0.05, 2.03, 1.63, 0.71, 0.70, 0.64, 0.36, 0.32, 0.20, 0.25, 0.12, 0.08, 2.72, 1.49, 1.16, 0.80, 0.80, 0.39, 0.22, 0.12, 0.11, 0.08, 0.08, 1.85, 1.39, 1.02, 0.89, 0.59, 0.40, 0.16, 0.11, 0.10, 0.07, 0.07, 2.05, 1.04, 0.81, 0.39, 0.30, 0.23, 0.13, 0.11, 0.08, 0.10, 0.06, 2.31, 1.44, 1.03, 0.84, 0.64, 0.42, 0.24, 0.17, 0.13, 0.10, 0.09.
For this data, Table 6 provides a summary of the numerical results of the parametric and non-parametric tests based on the MLEs of all comparison distributions. At a level of significance of α = 0.05 , it is possible to demonstrate that all distributions fit the plasma concentrations of the indomethicin data based on the p-value related to the K-S test. Since the GNEWD has the lowest value based on the parametric tests AIC and BIC, it is clear from Table 6 that it fits this data better than other distributions. Based on the plasma concentrations of the indomethicin data, Figure 5 displays the log-likelihood function profiles for each parameter. The approximate 95% CIs for λ , γ , a, and b are [1.2896, 2.1171], [0.5794, 0.9607], [0, 0.0004], and [1.9355, 5.4211], respectively, derived using the asymptotic variance–covariance matrix based on the MLEs for this data. The values of K-S and the corresponding p-value for the plasma concentrations of the indomethicin data are also shown in Table 7, along with all estimations of the unknown parameters based on the different methodologies that were considered in the previous section. When the K-S test is employed with the corresponding p-value, it is evident from Table 7 that the LSE is the optimal method for the plasma concentrations of the indomethicin data.

7. Simulation Study

The performance of various estimating techniques, as detailed in Section 5, is examined for the simulation study using the MSE and the AAB. In order to evaluate how well different approaches work in estimating the unknown parameters of the GNEWD, the following procedure is used:
  • Choose different values for the initial values of the parameters of the proposed distribution.
  • Generate random samples from the inverse CDF of the GNEWD with size n = (20, 60, 100, 150, 200, 250, 300).
  • Calculate the estimates for all the varying methods shown in Section 5.
  • Repeat Steps 2 and 3 N = 2000 times.
  • Calculate the MSEs and AABs.
All numerical results obtained from the simulation study for the different estimation methods are presented in Table 8, Table 9, Table 10 and Table 11. Upon examination of these tables, several notable patterns and findings emerge. Specifically, Table 8, Table 9, Table 10 and Table 11 illustrate the following:
  • The MSEs and the AABs for all methods of estimation decrease by increasing the sample size n.
  • The MLE and A-DE are superior to other estimating techniques based on MSE and AAB.

8. Conclusions

In this paper, a new extension of the Weibull distribution was proposed. It extended the new extended Weibull distribution by introducing an additional shape parameter, allowing it to capture more complex hazard rate patterns, including upside-down bathtub, and modified upside-down bathtub behaviors commonly observed in medical fields. The quantile of the GNEWD was calculated in closed form while the formula of moments could not be given in closed form. The estimation of the unknown parameters for the GNEWD using several estimating techniques, such as MLE, LSE, WLSE, CVME, and ADE, was introduced in this study. The GNEWD was applied to two real data sets in order to demonstrate how broadly it can be used in medical fields. The use of the parametric and non-parametric tests gives the GNEWD a competitive advantage when modeling lifetime data. Additionally, the simulation study was presented to compare the proposed estimation techniques employing MSEs and AABs. For future work, additional properties for the GNEWD can be studied including reliability analysis and entropy. Further, we will try to extend the proposed methods using different censoring schemes. Furthermore, the unknown parameters can be estimated by Bayesian estimation under complete and censoring data.

Author Contributions

Conceptualization, K.S.S. and H.M.M.R.; Methodology, A.S.A.-M., K.S.S. and H.M.M.R.; Software, H.M.M.R.; Validation, A.S.A.-M. and H.M.M.R.; Formal analysis, K.S.S.; Investigation, K.S.S.; Resources, A.S.A.-M.; Data curation, H.M.M.R.; Writing—original draft, H.M.M.R.; Writing—review & editing, A.S.A.-M.; Visualization, H.M.M.R.; Supervision, K.S.S.; Funding acquisition, A.S.A.-M. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported and funded by the Deanship of Scientific Research at Imam Mohammad Ibn Saud Islamic University (IMSIU) (grant number IMSIU-DDRSP2501).

Data Availability Statement

All data supporting the findings of this study are included within the article.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

Abbreviations

CDFCumulative distribution function
PDFProbability density function
HRFHazard rate function
AICAkaike information criterion
BICBayesian information criterion
K-SKolmogorov–Smirnov
IWDInverse Weibull distribution
GIWDGeneralized inverse Weibull distribution
GIGWDGeneralized inverse generalized Weibull distribution
GNEWDGeneralized new extended Weibull distribution
NEWDNew extended Weibull distribution
RGNEWDReduced generalized new extended Weibull distribution
RNEWDReduced new extended Weibull distribution
WDWeibull distribution
GMWDGeneralized Modified Weibull distribution
EWDExponentiated Weibull distribution
M-O WDMarshall–Olkin Weibull distribution
Logistic NHDLogistic Nadarajah–Haghighi distribution
IGLED              Inverted generalized linear exponential distribution
MLEMaximum likelihood estimation
LSELeast square estimation
WLSEWeighted least square estimation
CVMECramér Von-Mises estimation
ADEAnderson Darling estimation
ACIApproximate confidence interval

Appendix A

The second derivative of (14) with respect to the unknown parameters can be given as follows:
2 λ 2 = n λ 2 ,
2 λ γ = i = 1 n x i γ log x i e a x i b ,
2 λ a = i = 1 n e a x i b x i γ b ,
2 λ b = i = 1 n a log x i e a x i b x i γ b ,
2 γ 2 = i = 1 n 1 a b x i b + γ 2 i = 1 n λ x i γ log 2 x i e a x i b ,
2 γ a = i = 1 n b x i b a b x i b + γ 2 i = 1 n λ log x i e a x i b x i γ b ,
2 γ b = i = 1 n a b x i b log x i a b x i b + γ 2 a x i b a b x i b + γ 2 i = 1 n a λ log 2 x i e a x i b x i γ b ,
2 a 2 = i = 1 n b 2 x i 2 b a b x i b + γ 2 i = 1 n λ e a x i b x i γ 2 b ,
2 a b = i = 1 n x i b a b x i b + γ + b x i b a b x i b log x i a b x i b + γ 2 a x i b a b x i b + γ 2 b x i b log x i a b x i b + γ i = 1 n x i b log x i i = 1 n λ log x i e a x i b x i γ b a λ log x i e a x i b x i γ 2 b ,
2 b 2 = i = 1 n a b x i b log 2 x i 2 a x i b log x i a b x i b + γ + a x i b a b x i b log x i a b x i b log x i a b x i b + γ 2 a x i b a b x i b + γ 2 i = 1 n a x i b log 2 x i i = 1 n a 2 λ log 2 x i e a x i b x i γ 2 b a λ log 2 x i e a x i b x i γ b .

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Figure 1. The PDFs of GNEWD with different values of parameters.
Figure 1. The PDFs of GNEWD with different values of parameters.
Axioms 14 00490 g001
Figure 2. (a) The CDFs of GNEWD with different values of parameters; (b) the survival functions of GNEWD with different values of parameters.
Figure 2. (a) The CDFs of GNEWD with different values of parameters; (b) the survival functions of GNEWD with different values of parameters.
Axioms 14 00490 g002
Figure 3. The HRFs of GNEWD with different values of parameters.
Figure 3. The HRFs of GNEWD with different values of parameters.
Axioms 14 00490 g003
Figure 4. The profile of log-likelihood function of all parameters for the liver cancer data.
Figure 4. The profile of log-likelihood function of all parameters for the liver cancer data.
Axioms 14 00490 g004
Figure 5. The profile of log-likelihood function of all parameters for the plasma concentrations of indomethicin data.
Figure 5. The profile of log-likelihood function of all parameters for the plasma concentrations of indomethicin data.
Axioms 14 00490 g005
Table 1. The sub-models from GNEWD.
Table 1. The sub-models from GNEWD.
Distribution λ γ abCDFReference
NEWD ( λ , γ , a ) ---1 1 e λ x γ e a x 1 [8]
WD ( λ , γ ) --00 1 e λ x γ [1]
ED ( λ ) -100 1 e λ x [13]
RD ( c ) c 2 200 1 e c 2 x 2 [13]
RGNEWD ( λ , a , b ) - 1 2 -- 1 e λ x e a x b New
RNEWD ( λ , a ) - 1 2 -1 1 e λ x e a x 1 New
Table 2. The first four ordinary moments, variance, skewness, and kurtosis of the GNEWD using different values of a and b under fixed values of λ and γ .
Table 2. The first four ordinary moments, variance, skewness, and kurtosis of the GNEWD using different values of a and b under fixed values of λ and γ .
( λ , γ )ab μ 1 ( Θ ) μ 2 ( Θ ) μ 3 ( Θ ) μ 4 ( Θ ) Var ( Θ ) Sk ( Θ ) Kur ( Θ )
(1, 1)0.50.51.44733.588612.679858.16811.49390.07137.4830
0.511.38323.0239.373338.08331.1099−0.44858.0729
0.551.33762.45066.565324.77230.6614−1.627514.5145
0.5101.34682.43926.485724.52540.6253−1.874116.0129
0.5201.35562.44946.488824.51030.6118−2.051016.5705
20.52.884911.906463.9485422.0343.5836−2.22415.5169
60.57.445669.6021777.71810052.814.1651−6.83164.096
120.515.9514301.246515.96157785.46.7928−11.99943.5161
(3, 3)0.50.50.74810.6220.56050.53870.0624−26.76712.7259
0.510.76730.64210.57610.54750.0533−36.59332.7415
0.550.87890.78810.72120.67410.0156−348.6823.5212
0.5100.92910.86970.82070.78140.0065−1521.185.5792
0.5200.9630.93010.90130.87670.0027−6198.5212.7795
20.51.14281.41051.85112.5560.1045−44.17512.7403
60.52.28075.470213.682535.47330.2686−85.36072.8100
120.54.221618.490983.5819388.2940.6690−137.7252.8969
Table 3. Some unimodal well-known distributions.
Table 3. Some unimodal well-known distributions.
DistributionCDFReference
GMWD ( λ , γ , a , b ) ( 1 e λ x γ e a x ) b [19]
GIGWD ( λ , γ , a , b ) 1 ( 1 e γ ( λ x ) a ) b [20]
GIWD ( λ , γ , a ) e γ ( λ x ) a [21]
EWD ( λ , γ , a ) 1 e λ x γ a [2]
M-O WD ( λ , γ , a ) 1 a e λ x γ 1 ( 1 a ) e λ x γ [22]
Logistic NHD ( λ , γ , a ) ( λ x + 1 ) γ 1 a ( λ x + 1 ) γ 1 a + 1 [23]
IGLED ( λ , γ , a ) e γ 2 x 2 + λ x a [24]
IWD ( λ , γ ) e λ x γ [25]
Table 4. The ML estimates of unknown parameters, the K-S with the corresponding p-value, the AIC, and the BIC for different models using the liver cancer data.
Table 4. The ML estimates of unknown parameters, the K-S with the corresponding p-value, the AIC, and the BIC for different models using the liver cancer data.
Distribution λ ^ γ ^ a ^ b ^ K-S Distancep-ValueAICBIC
GNEWD ( λ , γ , a , b ) 0.01631.070142749.24.02870.08910.9160368.81375.46
NEWD ( λ , γ , a ) 0.10980.719626.3715-0.13500.4756374.52379.51
WD ( λ , γ ) 0.00391.3942--0.16570.2347378.56381.89
RGNEWD ( λ , a , b ) 0.2497-91.87781.41090.10810.7521374.73379.72
RNEWD ( λ , a ) 0.3175-33.6649-0.12710.5542373.05376.37
GMWD ( λ , γ , a , b ) 19.76180.04900.0004 1.5379 × 10 10 0.13040.5209375.76382.41
GIGWD ( λ , γ , a , b ) 5.060910.44341.37111.20490.11790.6493377.64384.29
GIWD ( λ , γ , a ) 4.293614.79421.5307-0.11330.6986375.65380.64
EWD ( λ , γ , a ) 6.31190.145825387.1-0.12420.5846375.29380.29
M-O WD ( λ , γ , a ) 0.00021.88120.1801-0.13730.4546378.16383.15
Logistic NHD ( λ , γ , a ) 0.73790.21225.2217-0.12700.5554379.49384.49
IGLED ( λ , γ , a ) 23.173075.06971.4495-0.11210.7112375.56380.55
IWD ( λ , γ ) 137.631.5306--0.11330.6986373.65376.98
Table 5. Unknown parameter estimates using different approaches and the K-S test with the associated p-value for the liver cancer data.
Table 5. Unknown parameter estimates using different approaches and the K-S test with the associated p-value for the liver cancer data.
Methods λ ^ γ ^ a ^ b ^ K-S Distancep-Value
MLE0.01631.070142749.24.02870.08910.9160
LSE0.02790.9156 2.1 × 10 6 5.48090.08870.9187
WLSE0.01881.0191 7.01 × 10 7 6.81390.07710.9745
CVME0.02540.9428 3.3 × 10 6 5.61720.08070.9614
ADE0.02270.977186756.894.31040.07170.9881
Table 6. The ML estimates of unknown parameters, the K-S with the corresponding p-value, the AIC, and the BIC for different models using the plasma concentrations of indomethicin data.
Table 6. The ML estimates of unknown parameters, the K-S with the corresponding p-value, the AIC, and the BIC for different models using the plasma concentrations of indomethicin data.
Distribution λ ^ γ ^ a ^ b ^ K-S Distancep-ValueAICBIC
GNEWD ( λ , γ , a , b ) 1.70330.77000.00013.67830.08150.773045.4354.18
NEWD ( λ , γ , a ) 1.97870.61450.1092-0.13220.199256.3362.90
WD ( λ , γ ) 1.68570.9546--0.13480.181766.5170.89
RGNEWD ( λ , a , b ) 1.6526-0.00122.73400.10640.443352.0658.63
RNEWD ( λ , a ) 2.0325-0.1332-0.11730.324355.1959.57
GMWD ( λ , γ , a , b ) 24.81990.03240.0251 2.02768 × 10 10 0.13270.195658.6667.42
GIGWD ( λ , γ , a , b ) 1.13120.80820.55153.33380.13480.181764.3273.08
GIWD ( λ , γ , a ) 0.57150.32121.0196-0.11480.349462.9269.49
EWD ( λ , γ , a ) 8.24270.1495660.96-0.12990.214761.7368.29
M-O WD ( λ , γ , a ) 0.70831.26910.1985-0.13270.195665.0571.62
Logistic NHD ( λ , γ , a ) 0.35945.50971.0471-0.136040.173768.2874.85
IGLED ( λ , γ , a ) 0.16960.00470.9568-0.11190.379362.5269.08
IWD ( λ , γ ) 0.18161.0196--0.11480.349460.9265.29
Table 7. Unknown parameter estimates using different approaches and the K-S test with the associated P-value for the plasma concentrations of indomethicin data.
Table 7. Unknown parameter estimates using different approaches and the K-S test with the associated P-value for the plasma concentrations of indomethicin data.
Methods λ ^ γ ^ a ^ b ^ K-S Distancep-Value
MLE1.70330.77000.00013.67830.08150.7730
LSE1.53530.6966 1.2 × 10 6 5.25770.05290.9925
WLSE1.60490.7416 1.5 × 10 6 5.15120.06380.9513
CVME1.55690.7097 8.7 × 10 7 5.42230.05580.9863
ADE1.60880.7343 1.4 × 10 5 4.28030.06750.9244
Table 8. MSEs and AAB for parameter γ under proposed methods with varying sample size n.
Table 8. MSEs and AAB for parameter γ under proposed methods with varying sample size n.
n ( γ , λ , b , a ) MLELSEWLSECVMEADE
20 ( 0.8 , 0.4 , 1.5 , 0.2 ) MSE0.03570.08050.11740.05780.036
AAB0.14210.17030.18320.15310.1455
( 0.8 , 0.4 , 3.5 , 0.2 ) MSE0.02850.06290.12490.05060.0381
AAB0.13140.20590.20190.17760.1532
60 ( 0.8 , 0.4 , 1.5 , 0.2 ) MSE0.01350.02550.02160.02050.0168
AAB0.09140.12320.11540.11070.0994
( 0.8 , 0.4 , 3.5 , 0.2 ) MSE0.0120.02370.01750.02010.0145
AAB0.08390.12270.10310.11190.0922
100 ( 0.8 , 0.4 , 1.5 , 0.2 ) MSE0.01050.01910.01460.01540.0116
AAB0.07920.10520.0930.09550.0815
( 0.8 , 0.4 , 3.5 , 0.2 ) MSE0.00890.01430.00970.0130.0088
AAB0.07090.0930.07610.08860.0717
150 ( 0.8 , 0.4 , 1.5 , 0.2 ) MSE0.00830.01540.010.01280.0091
AAB0.06860.09290.07640.08560.0729
( 0.8 , 0.4 , 3.5 , 0.2 ) MSE0.00740.00930.00620.00870.0059
AAB0.06230.07430.06070.07190.0584
200 ( 0.8 , 0.4 , 1.5 , 0.2 ) MSE0.00830.01390.00870.01190.008
AAB0.06720.08880.07100.08310.0678
( 0.8 , 0.4 , 3.5 , 0.2 ) MSE0.00620.00670.00430.00650.0043
AAB0.05690.06280.05050.06180.0499
250 ( 0.8 , 0.4 , 1.5 , 0.2 ) MSE0.00720.01240.25790.01120.0063
AAB0.06030.08210.06050.07840.0602
( 0.8 , 0.4 , 3.5 , 0.2 ) MSE0.00540.00600.00360.00530.0040
AAB0.05360.05840.04680.05550.0472
300 ( 0.8 , 0.4 , 1.5 , 0.2 ) MSE0.00730.01110.00570.00990.0058
AAB0.06010.07890.05840.07550.0580
( 0.8 , 0.4 , 3.5 , 0.2 ) MSE0.00480.00450.00280.00450.0032
AAB0.04970.05080.04120.05050.0415
Table 9. MSEs and AAB for parameter λ under proposed methods with varying sample size n.
Table 9. MSEs and AAB for parameter λ under proposed methods with varying sample size n.
n ( γ , λ , b , a ) MLELSEWLSECVMEADE
20 ( 0.8 , 0.4 , 1.5 , 0.2 ) MSE0.03610.04810.0550.02670.0324
AAB0.13510.13550.14930.11060.1194
( 0.8 , 0.4 , 3.5 , 0.2 ) MSE0.02470.06930.06790.04640.0396
AAB0.11310.18090.17630.15120.1378
60 ( 0.8 , 0.4 , 1.5 , 0.2 ) MSE0.02440.04090.03720.02420.0251
AAB0.10260.12110.12150.09870.1005
( 0.8 , 0.4 , 3.5 , 0.2 ) MSE0.01090.02730.01690.02110.0145
AAB0.07270.10780.08980.0970.0826
100 ( 0.8 , 0.4 , 1.5 , 0.2 ) MSE0.0180.03850.02670.02140.019
AAB0.08820.11250.10180.09120.0857
( 0.8 , 0.4 , 3.5 , 0.2 ) MSE0.00810.0150.00790.01220.0081
AAB0.06000.07820.06310.07290.0614
150 ( 0.8 , 0.4 , 1.5 , 0.2 ) MSE0.01550.03430.01760.02050.0147
AAB0.07610.10540.08240.0880.0756
( 0.8 , 0.4 , 3.5 , 0.2 ) MSE0.00630.00940.00510.00810.55
AAB0.05370.06250.05070.05970.0492
200 ( 0.8 , 0.4 , 1.5 , 0.2 ) MSE0.0160.03370.01460.02180.0136
AAB0.07470.10190.07470.08710.0714
( 0.8 , 0.4 , 3.5 , 0.2 ) MSE0.00480.0060.0030.00590.0035
AAB0.04760.05040.04120.04950.0415
250 ( 0.8 , 0.4 , 1.5 , 0.2 ) MSE0.01470.03170.00870.02370.0094
AAB0.06690.09540.06130.08600.0622
( 0.8 , 0.4 , 3.5 , 0.2 ) MSE0.00430.00580.00240.00490.0030
AAB0.04440.04660.03750.04390.0386
300 ( 0.8 , 0.4 , 1.5 , 0.2 ) MSE0.01630.02590.00750.01880.0082
AAB0.06800.09180.05850.08200.0594
( 0.8 , 0.4 , 3.5 , 0.2 ) MSE0.00390.00410.00190.00410.0030
AAB0.04110.04030.03340.04040.0345
Table 10. MSEs and AAB for parameter b under proposed methods with varying sample size n.
Table 10. MSEs and AAB for parameter b under proposed methods with varying sample size n.
n ( γ , λ , b , a ) MLELSEWLSECVMEADE
20 ( 0.8 , 0.4 , 1.5 , 0.2 ) MSE0.94140.74070.69260.87870.5949
AAB0.83560.68130.65550.74730.5953
( 0.8 , 0.4 , 3.5 , 0.2 ) MSE1.24762.22612.10381.92851.3228
AAB0.89861.1631.14441.09230.9141
60 ( 0.8 , 0.4 , 1.5 , 0.2 ) MSE0.57660.64680.47780.71730.3704
AAB0.59670.64530.54520.66820.4679
( 0.8 , 0.4 , 3.5 , 0.2 ) MSE0.80351.46011.13291.38740.9445
AAB0.72930.9750.84830.95590.7774
100 ( 0.8 , 0.4 , 1.5 , 0.2 ) MSE0.44570.58120.39480.63970.289
AAB0.51570.60740.49580.63050.418
( 0.8 , 0.4 , 3.5 , 0.2 ) MSE0.6821.17350.76421.17460.7257
AAB0.66170.87640.70480.87840.6773
150 ( 0.8 , 0.4 , 1.5 , 0.2 ) MSE0.38070.52730.33080.54680.2521
AAB0.46620.5760.44630.5810.3926
( 0.8 , 0.4 , 3.5 , 0.2 ) MSE0.57420.96480.59990.97910.55
AAB0.58840.78680.61260.78790.5798
200 ( 0.8 , 0.4 , 1.5 , 0.2 ) MSE0.31870.49780.30270.52250.2321
AAB0.42480.55450.42090.56140.3758
( 0.8 , 0.4 , 3.5 , 0.2 ) MSE0.50630.82080.49000.89650.4902
AAB0.56000.73500.56430.76310.5523
250 ( 0.8 , 0.4 , 1.5 , 0.2 ) MSE0.25450.46940.25790.48840.2083
AAB0.38050.54270.39290.54930.3608
( 0.8 , 0.4 , 3.5 , 0.2 ) MSE0.42220.74090.42450.70820.4339
AAB0.50310.68810.52480.67660.5164
300 ( 0.8 , 0.4 , 1.5 , 0.2 ) MSE0.24190.44120.23520.45630.2006
AAB0.36480.53230.37400.53610.3480
( 0.8 , 0.4 , 3.5 , 0.2 ) MSE0.36250.64780.36500.66500.3847
AAB0.46140.63430.47760.64090.4717
Table 11. MSEs and AAB for parameter a under proposed methods with varying sample size n.
Table 11. MSEs and AAB for parameter a under proposed methods with varying sample size n.
n ( γ , λ , b , a ) MLELSEWLSECVMEADE
20 ( 0.8 , 0.4 , 1.5 , 0.2 ) MSE0.1340.07540.0920.0540.0711
AAB0.25450.18240.20030.16050.1768
( 0.8 , 0.4 , 3.5 , 0.2 ) MSE0.08850.15790.15260.13210.1019
AAB0.19540.27490.26750.25350.2159
60 ( 0.8 , 0.4 , 1.5 , 0.2 ) MSE0.08530.09890.09060.0660.0672
AAB0.19480.20840.20190.17680.1729
( 0.8 , 0.4 , 3.5 , 0.2 ) MSE0.04230.0970.06550.08390.0622
AAB0.13490.20650.17580.19520.1663
100 ( 0.8 , 0.4 , 1.5 , 0.2 ) MSE0.0640.0970.07680.06440.0625
AAB0.16970.20320.18450.17540.1632
( 0.8 , 0.4 , 3.5 , 0.2 ) MSE0.03220.06210.03560.05510.0411
AAB0.11620.1630.12930.15550.1319
150 ( 0.8 , 0.4 , 1.5 , 0.2 ) MSE0.0550.09220.05730.06560.0522
AAB0.15380.19820.15970.17410.1518
( 0.8 , 0.4 , 3.5 , 0.2 ) MSE0.02560.04210.02250.03980.0257
AAB0.10060.13090.10270.12840.1031
200 ( 0.8 , 0.4 , 1.5 , 0.2 ) MSE0.05470.09180.05050.06940.0492
AAB0.15210.19510.15090.17640.1481
( 0.8 , 0.4 , 3.5 , 0.2 ) MSE0.02020.03010.01420.03160.0184
AAB0.09040.11280.08630.11580.0899
250 ( 0.8 , 0.4 , 1.5 , 0.2 ) MSE0.04620.08680.03360.07140.0404
AAB0.13370.18450.12750.17210.1357
( 0.8 , 0.4 , 3.5 , 0.2 ) MSE0.01830.02840.01190.02470.0173
AAB0.08280.10570.07900.10090.0850
300 ( 0.8 , 0.4 , 1.5 , 0.2 ) MSE0.05210.07900.03100.06360.0368
AAB0.13650.18500.12450.17080.1310
( 0.8 , 0.4 , 3.5 , 0.2 ) MSE0.01690.02030.00860.02100.0156
AAB0.07770.09060.06930.09070.0760
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Al-Moisheer, A.S.; Sultan, K.S.; Radwan, H.M.M. A Novel Adaptable Weibull Distribution and Its Applications. Axioms 2025, 14, 490. https://doi.org/10.3390/axioms14070490

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Al-Moisheer AS, Sultan KS, Radwan HMM. A Novel Adaptable Weibull Distribution and Its Applications. Axioms. 2025; 14(7):490. https://doi.org/10.3390/axioms14070490

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Al-Moisheer, Asmaa S., Khalaf S. Sultan, and Hossam M. M. Radwan. 2025. "A Novel Adaptable Weibull Distribution and Its Applications" Axioms 14, no. 7: 490. https://doi.org/10.3390/axioms14070490

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Al-Moisheer, A. S., Sultan, K. S., & Radwan, H. M. M. (2025). A Novel Adaptable Weibull Distribution and Its Applications. Axioms, 14(7), 490. https://doi.org/10.3390/axioms14070490

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